De la Mare, P B D’s team published research in Journal of the Chemical Society in 1957 | 16426-64-5

Journal of the Chemical Society published new progress about Bromination. 16426-64-5 belongs to class bromides-buliding-blocks, and the molecular formula is C7H4BrNO4, Category: bromides-buliding-blocks.

De la Mare, P. B. D.; Harvey, J. T. published the artcile< Kinetics and mechanisms of aromatic halogen substitution. III. Partial rate factors for the acid-catalyzed bromination of tert-butylbenzene by hypobromous acid>, Category: bromides-buliding-blocks, the main research area is .

The products of acid-catalyzed reaction of tert-BuPh (I) with HOBr in 50% aqueous dioxane were determined, by isotopic dilution, as 37.7% o- (II), 7.2%, m- (III), and 53.2% p-BrC6H4Bu-tert (IV), and 1.9% PhBr (V). Negligible side chain substitution accompanied the reaction, the kinetic form of which was -d[BrOH]/dt = k[ArH][BrOH][H+], with k = 435 1.2 mole-2 min.-1 at 25°, 12 times greater than for C6H6. These results showed that, in a comparison of I with PhMe, the p-position was less reactive, and the m-position was about equally reactive. Significant electrophilic displacement of the tert-Bu group by Br occurred during the reaction. The results were discussed with special reference to the hyperconjugative power of alkyl groups, and to the effect of steric hindrance in determining the reactivity of the o-position. Some nitro derivatives of II, III, and IV were described. III b10 95-7°, nD25 1.5335 and II, b14 102°, nD25 1.5410. II heated at 80° with 1.5 equivalents 98% HNO3 in a mixture of 35% volume/volume H2SO4 and AcOH and the product chromatographed in C6H6 on Al2O3 gave 2,5-Br(O2N)C6H3Bu-tert (VI). The position of the NO2 group was proved as follows: VI (7.5 g.) heated 50 hrs. at 160° with 30% HNO3 in 3 sealed tubes gave about 3% 2,5-Br(O2N)C6H4CO2H, m. 181°. Model experiments showed that 2,4-Br(O2N)C6H3Bu-tert was similarly oxidized to 2,4-Br(O2N)C6H4CO2H, m. 166°. III heated at 80° with 2 equivalents HNO3 in H2SO4435AcOH similarly gave 30% 5,2 (?),4-Br(O2N)2C6H2Bu-tert, m. 92° (from C5H12). IV (5 g.) similarly heated 6 hrs. at 80° under the same nitrating conditions gave a small yield of p-BrC6H4NO2, m. 124°. In the study of the kinetics of bromination the following was a typical run: from a mixture of I (0.00564M), 0.0028M HOBr, and 0.0221M HClO4 in 50% dioxane, aliquot parts were removed at intervals for titration. A blank run with I omitted was made side by side with this measurement. The mean value of k was found to be 435 l.2 mole-2 min.-1 Labeled IV was prepared, NH4Br82 being first shaken with the Br used in the reaction. The product had f.p. 15.7°. To a solution of 10 l. HOBr and 0.05M HClO4 in 50% dioxane was added 19.18 g. I, then 2.37 g. labeled IV was added to the mixture, the mixture extracted with Et2O, and the IV crystallized to give by calculation 9.19 g. IV. Similarly it was shown that 0.308 g. II had been produced in the reaction. III was treated as for II. The mixture contained 0.843 g. active bromo-tert-butylbenzenes, to which was added 11.45 g. inactive III, and the mixture counted, showing that 0.0606 g. III was produced in the reaction. To a mixture which should have contained 1.36 g. mixed active bromo-tert-butylbenzenes was added 12.74 g. V; the mixture extracted, the product nitrated for 2-3 hrs. at 80°, and the product recovered and chromatographed showed that the reaction mixture contained 0.0197 g. V. The conclusion that there was greater hindrance to the entry of NO2 than of Br o- to an alkyl group, was confirmed by this investigation. For I the rate ratios were 0.37 and 0.07, resp., and the free energy difference corresponding to these figures was 0.87 kcal./mole. The effects of hyperconjugation in PhMe and I were considered in some detail. The small proportion of V (1.9 mole-%) determined in the products of bromination was considered significant. The absolute rate of displacement of a tert-Bu group from I was faster than that of displacement of a proton from C6H8.

Journal of the Chemical Society published new progress about Bromination. 16426-64-5 belongs to class bromides-buliding-blocks, and the molecular formula is C7H4BrNO4, Category: bromides-buliding-blocks.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

De la Mare, P B D’s team published research in Journal of the Chemical Society in 1957 | 16426-64-5

Journal of the Chemical Society published new progress about Bromination. 16426-64-5 belongs to class bromides-buliding-blocks, and the molecular formula is C7H4BrNO4, Category: bromides-buliding-blocks.

De la Mare, P. B. D.; Harvey, J. T. published the artcile< Kinetics and mechanisms of aromatic halogen substitution. III. Partial rate factors for the acid-catalyzed bromination of tert-butylbenzene by hypobromous acid>, Category: bromides-buliding-blocks, the main research area is .

The products of acid-catalyzed reaction of tert-BuPh (I) with HOBr in 50% aqueous dioxane were determined, by isotopic dilution, as 37.7% o- (II), 7.2%, m- (III), and 53.2% p-BrC6H4Bu-tert (IV), and 1.9% PhBr (V). Negligible side chain substitution accompanied the reaction, the kinetic form of which was -d[BrOH]/dt = k[ArH][BrOH][H+], with k = 435 1.2 mole-2 min.-1 at 25°, 12 times greater than for C6H6. These results showed that, in a comparison of I with PhMe, the p-position was less reactive, and the m-position was about equally reactive. Significant electrophilic displacement of the tert-Bu group by Br occurred during the reaction. The results were discussed with special reference to the hyperconjugative power of alkyl groups, and to the effect of steric hindrance in determining the reactivity of the o-position. Some nitro derivatives of II, III, and IV were described. III b10 95-7°, nD25 1.5335 and II, b14 102°, nD25 1.5410. II heated at 80° with 1.5 equivalents 98% HNO3 in a mixture of 35% volume/volume H2SO4 and AcOH and the product chromatographed in C6H6 on Al2O3 gave 2,5-Br(O2N)C6H3Bu-tert (VI). The position of the NO2 group was proved as follows: VI (7.5 g.) heated 50 hrs. at 160° with 30% HNO3 in 3 sealed tubes gave about 3% 2,5-Br(O2N)C6H4CO2H, m. 181°. Model experiments showed that 2,4-Br(O2N)C6H3Bu-tert was similarly oxidized to 2,4-Br(O2N)C6H4CO2H, m. 166°. III heated at 80° with 2 equivalents HNO3 in H2SO4435AcOH similarly gave 30% 5,2 (?),4-Br(O2N)2C6H2Bu-tert, m. 92° (from C5H12). IV (5 g.) similarly heated 6 hrs. at 80° under the same nitrating conditions gave a small yield of p-BrC6H4NO2, m. 124°. In the study of the kinetics of bromination the following was a typical run: from a mixture of I (0.00564M), 0.0028M HOBr, and 0.0221M HClO4 in 50% dioxane, aliquot parts were removed at intervals for titration. A blank run with I omitted was made side by side with this measurement. The mean value of k was found to be 435 l.2 mole-2 min.-1 Labeled IV was prepared, NH4Br82 being first shaken with the Br used in the reaction. The product had f.p. 15.7°. To a solution of 10 l. HOBr and 0.05M HClO4 in 50% dioxane was added 19.18 g. I, then 2.37 g. labeled IV was added to the mixture, the mixture extracted with Et2O, and the IV crystallized to give by calculation 9.19 g. IV. Similarly it was shown that 0.308 g. II had been produced in the reaction. III was treated as for II. The mixture contained 0.843 g. active bromo-tert-butylbenzenes, to which was added 11.45 g. inactive III, and the mixture counted, showing that 0.0606 g. III was produced in the reaction. To a mixture which should have contained 1.36 g. mixed active bromo-tert-butylbenzenes was added 12.74 g. V; the mixture extracted, the product nitrated for 2-3 hrs. at 80°, and the product recovered and chromatographed showed that the reaction mixture contained 0.0197 g. V. The conclusion that there was greater hindrance to the entry of NO2 than of Br o- to an alkyl group, was confirmed by this investigation. For I the rate ratios were 0.37 and 0.07, resp., and the free energy difference corresponding to these figures was 0.87 kcal./mole. The effects of hyperconjugation in PhMe and I were considered in some detail. The small proportion of V (1.9 mole-%) determined in the products of bromination was considered significant. The absolute rate of displacement of a tert-Bu group from I was faster than that of displacement of a proton from C6H8.

Journal of the Chemical Society published new progress about Bromination. 16426-64-5 belongs to class bromides-buliding-blocks, and the molecular formula is C7H4BrNO4, Category: bromides-buliding-blocks.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Bolchi, Cristiano’s team published research in Bioorganic & Medicinal Chemistry Letters in 2007-11-15 | 16426-64-5

Bioorganic & Medicinal Chemistry Letters published new progress about Antiatherosclerotics. 16426-64-5 belongs to class bromides-buliding-blocks, and the molecular formula is C7H4BrNO4, Safety of 2-Bromo-4-nitrobenzoic acid.

Bolchi, Cristiano; Pallavicini, Marco; Rusconi, Chiara; Diomede, Luisa; Ferri, Nicola; Corsini, Alberto; Fumagalli, Laura; Pedretti, Alessandro; Vistoli, Giulio; Valoti, Ermanno published the artcile< Peptidomimetic inhibitors of farnesyltransferase with high in vitro activity and significant cellular potency>, Safety of 2-Bromo-4-nitrobenzoic acid, the main research area is peptidomimetic inhibitor farnesyltransferase antiproliferative aorta smooth muscle atherosclerosis.

2-O-Tolyl or 2-o-anisyl substituted 4-hydroxy- and 4-carboxybenzamides of methionine, etherified and amidified with 2-hydroxymethyl- and 2-aminomethylpyridodioxane, resp., are described as inhibitors of Ras protein farnesyltransferase (FTase). Of the sixteen compounds, resulting from the substitution pattern of benzamide and the configuration of the two stereocenters, seven inhibited FTase activity with potencies in the nanomolar range. They were all 2-oxymethylpyridodioxane ethers and, among them, the four o-tolyl substituted stereoisomers also showed micromolar antiproliferative effect on human aortic smooth muscle cells interfering with Ras farnesylation. The docking anal. enlightened significant differences in enzyme interaction between oxymethylpyridodioxane and aminomethylpyridodioxane derivatives

Bioorganic & Medicinal Chemistry Letters published new progress about Antiatherosclerotics. 16426-64-5 belongs to class bromides-buliding-blocks, and the molecular formula is C7H4BrNO4, Safety of 2-Bromo-4-nitrobenzoic acid.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Toledo-Sherman, Leticia’s team published research in Journal of Medicinal Chemistry in 2019-03-28 | 16426-64-5

Journal of Medicinal Chemistry published new progress about Crystal structure (X-ray structure of 33 bound to the mutant Vps34 construct). 16426-64-5 belongs to class bromides-buliding-blocks, and the molecular formula is C7H4BrNO4, Synthetic Route of 16426-64-5.

Toledo-Sherman, Leticia; Breccia, Perla; Cachope, Roger; Bate, Jennifer R.; Angulo-Herrera, Ivan; Wishart, Grant; Matthews, Kim L.; Martin, Sarah L.; Cox, Helen C.; McAllister, George; Penrose, Stephen D.; Vater, Huw; Esmieu, William; Van de Poel, Amanda; Van de Bospoort, Rhea; Strijbosch, Annelieke; Lamers, Marieke; Leonard, Philip; Jarvis, Rebecca E.; Blackaby, Wesley; Barnes, Karen; Eznarriaga, Maria; Dowler, Simon; Smith, Graham D.; Fischer, David F.; Lazari, Ovadia; Yates, Dawn; Rose, Mark; Jang, Sung-Wook; Munoz-Sanjuan, Ignacio; Dominguez, Celia published the artcile< Optimization of Potent and Selective Ataxia Telangiectasia-Mutated Inhibitors Suitable for a Proof-of-Concept Study in Huntington's Disease Models>, Synthetic Route of 16426-64-5, the main research area is ATM inhibitor Huntington’s disease mHTT PK PD brain penetrant.

Genetic and pharmacol. evidence indicates that the reduction of ataxia telangiectasia-mutated (ATM) kinase activity can ameliorate mutant huntingtin (mHTT) toxicity in cellular and animal models of Huntington’s disease (HD), suggesting that selective inhibition of ATM could provide a novel clin. intervention to treat HD. Here, we describe the development and characterization of ATM inhibitor mols. to enable in vivo proof-of-concept studies in HD animal models. Starting from previously reported ATM inhibitors, we aimed with few modifications to increase brain exposure by decreasing P-glycoprotein liability while maintaining potency and selectivity. Here, we report brain-penetrant ATM inhibitors that have robust pharmacodynamic (PD) effects consistent with ATM kinase inhibition in the mouse brain and an understandable pharmacokinetic/PD (PK/PD) relationship. Compound 17 engages ATM kinase and shows robust dose-dependent inhibition of X-ray irradiation-induced KAP1 phosphorylation in the mouse brain. Furthermore, compound 17 protects against mHTT (Q73)-induced cytotoxicity in a cortical-striatal cell model of HD.

Journal of Medicinal Chemistry published new progress about Crystal structure (X-ray structure of 33 bound to the mutant Vps34 construct). 16426-64-5 belongs to class bromides-buliding-blocks, and the molecular formula is C7H4BrNO4, Synthetic Route of 16426-64-5.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Petrovich, P I’s team published research in Zhurnal Obshchei Khimii in 1960 | 16426-64-5

Zhurnal Obshchei Khimii published new progress about Nitration. 16426-64-5 belongs to class bromides-buliding-blocks, and the molecular formula is C7H4BrNO4, HPLC of Formula: 16426-64-5.

Petrovich, P. I. published the artcile< Oxidative nitration of aromatic compounds. IV. Mercury compounds of some p-disubstituted benzenes and their reaction with nitric acid>, HPLC of Formula: 16426-64-5, the main research area is .

Heating 200 g. p-C6H4Cl2, 40 g. Hg(OAc)2, 60 ml. AcOH, and 1 ml. petr. ether 11.5 hrs. at 125° gave 50% acetoxymercuri-p-dichlorobenzene (I) m. 168.5-9.2°, along with bis(2,5-dichlorophenyl)mercury (II), m. 235-7°. The former with NaCl gave the chloromercuri analog, m. 207-7.5°. Similar reaction of 100 g. p-C6H4Cl2 and 20 g. Hg(OAc)2 in AcOH in the presence of petr. ether in 13 hrs. gave a moderate yield of II, which was also formed by heating I in boiling xylene 10 hrs. I heated without solvent at 172° gave p-C6H4Cl2. II heated with HgCl2 in EtOH-C6H6 gave chloromercuri-p-dichlorobenzene. Oxidation of chloromercuri-p-xylene with KMnO4 in aqueous NaOH at 95° gave 85.3% anhydro-2-(hydroxymercuri)terephthalic acid (Whitmore and Isenhour, CA 23, 4943), which with Br-KBr gave bromoterephthalic acid, m. 298-8.7°. Diazotization of 4-nitro-2-aminotoluene and treatment with HgCl2 gave a colorless 2:1 complex of 4-nitro-2-toluenediazonium chloride and HgCl2, which on conventional decomposition gave 38.8% 2-chloromercuri-4-nitrotoluene, m. 231.5-2°, which with powd. Cu in NH4OH gave bis(4-nitro-2-tolyl)mercury, m. 258.2-8.6°, while oxidation of the former with KMnO4 gave 75% anhydro-2-(hydroxymercuri)-4-nitrobenzoic acid (Whitmore and Middleton, CA 16, 2856), which with Br-KBr gave 2-bromo-4-nitrobenzoic acid, m. 167-8°. I added gradually to 58% HNO3 at 75° and stirred 1.2 hrs. (N oxide formation was caused by gradual addition of paraformaldehyde) gave some 2,5-dichloronitrobenzene (III) and a low yield of 3,6-dichloro-2,4-dinitrophenol (IV), m. 146.2-7°. Similar treatment of II also gave the same product in low yield. Heating 36 g. p-C6H4Cl2, 276 ml. 58% HNO3, 36 g. Hg(NO3)2, 1.2 g. NaNO2, and 1 ml. petr. ether 25 hrs. at 80° gave low yields of III and IV. The above reaction mixture heated in a sealed tube 7 hrs. at 140° (petr. ether omitted) gave HgCl2, 2,5-dichloro-1,3-dinitrobenzene, 2,5-dichloro-1,4-dinitrobenzene and, as the principal product, III (yield not stated). Heating anhydro-2-(hydroxymercuri)terephthalic acid with 58% HNO3 and a trace of NaNO2 (as above) 7 hrs. at 80° in a sealed tube gave 30% nitroterephthalic acid, m. 267-8°. Heating 2-chloromercuri-4-nitrotoluene with 58% HNO3 2.5 hrs. at 50° in the presence of NaNO2 gave a little 2-nitroso-4-nitrotoluene and 2,4-(O2N)2C6H3Me.

Zhurnal Obshchei Khimii published new progress about Nitration. 16426-64-5 belongs to class bromides-buliding-blocks, and the molecular formula is C7H4BrNO4, HPLC of Formula: 16426-64-5.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Yanagi, Kouichi’s team published research in Cell Reports in 2021-07-06 | 16426-64-5

Cell Reports published new progress about Amino acids Role: BSU (Biological Study, Unclassified), BIOL (Biological Study). 16426-64-5 belongs to class bromides-buliding-blocks, and the molecular formula is C7H4BrNO4, Synthetic Route of 16426-64-5.

Yanagi, Kouichi; Komatsu, Toru; Ogihara, Shusuke; Okabe, Takayoshi; Kojima, Hirotatsu; Nagano, Tetsuo; Ueno, Tasuku; Hanaoka, Kenjiro; Urano, Yasuteru published the artcile< Establishment of live-cell-based coupled assay system for identification of compounds to modulate metabolic activities of cells>, Synthetic Route of 16426-64-5, the main research area is fluorescence imaging metabolic activity tumor cell glycolysis; chemical biology; coupled assays; fluorescent probes; glucolysis; glutaminolysis; metabolism.

In this study, we present a live-cell-based fluorometric coupled assay system to identify the compounds that can regulate the targeted metabolic pathways in live cells. The assay is established through targeting specific metabolic pathways and using “” input “” and “”output “” metabolite pairs. The changes in the extracellular output that are generated and released into the extracellular media from the input are assessed as the activity of the pathway. The screening for the glycolytic pathway and amino acid metabolism reveals the activities of the present drugs, 6-BIO and regorafenib, that regulate the metabolic fate of tumor cells.

Cell Reports published new progress about Amino acids Role: BSU (Biological Study, Unclassified), BIOL (Biological Study). 16426-64-5 belongs to class bromides-buliding-blocks, and the molecular formula is C7H4BrNO4, Synthetic Route of 16426-64-5.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Poornima, B’s team published research in Tetrahedron in 2016-08-11 | 16426-64-5

Tetrahedron published new progress about Antitumor agents. 16426-64-5 belongs to class bromides-buliding-blocks, and the molecular formula is C7H4BrNO4, Quality Control of 16426-64-5.

Poornima, B.; Venkanna, A.; Swetha, B.; Kamireddy, Karthik Reddy; Siva, Bandi; Phani Babu, V. S.; Ummanni, Ramesh; Babu, K. Suresh published the artcile< Total synthesis, biological evaluation of dendrodolides A-D and their analogues>, Quality Control of 16426-64-5, the main research area is dendrodolide synthesis anticancer.

A concise total synthesis of dendrodolides A-D has been accomplished in 10 steps from com. available (R)-propylene oxide and 3-buten-1-ol as starting materials. The key steps involved in the synthesis are Jacobsen hydrolytic kinetic resolution, epoxide ring opening with 2-allyl-1,3-dithiane, Yamaguchi esterification and ring-closing metathesis (RCM). In addition, a series of ester derivatives were prepared utilizing Yamaguchi esterification at the C-3 position of the dendrodolide core and screened for their efficacy against cancer cell lines.

Tetrahedron published new progress about Antitumor agents. 16426-64-5 belongs to class bromides-buliding-blocks, and the molecular formula is C7H4BrNO4, Quality Control of 16426-64-5.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Yokoyama, Akihiro’s team published research in Tetrahedron Letters in 2021-01-05 | 16426-64-5

Tetrahedron Letters published new progress about Arylation (intramol.). 16426-64-5 belongs to class bromides-buliding-blocks, and the molecular formula is C7H4BrNO4, Quality Control of 16426-64-5.

Yokoyama, Akihiro; Ishii, Arisa; Ohishi, Tomoyuki; Kikkawa, Shoko; Azumaya, Isao published the artcile< Synthesis of a coronene analogue containing an amide bond by Pd-mediated intramolecular C-C bond formation of 2-halogenated 4-(alkylamino)benzoic acid cyclic trimer>, Quality Control of 16426-64-5, the main research area is coronene amide synthesis palladium mediated intramol cyclization.

A coronene analog containing amide linkage was synthesized from a halogenated cyclic triamide by palladium-mediated intramol. C-C bond formation (I → II). The cyclic triamide was formed from the condensation of 2-chloro-4-(isobutylamino)benzoic acid in the presence of dichlorotriphenylphosphorane in 1,1,2,2-tetrachloroethane. By contrast, the condensation of 2-bromo counterpart required silicon tetrachloride in pyridine. The intramol. C-C bond formation, which yielded the target coronene analog, occurred during the reaction of bromo-substituted cyclic triamide with palladium(II) acetate, triphenylphosphine, and potassium carbonate in N,N-dimethylformamide.

Tetrahedron Letters published new progress about Arylation (intramol.). 16426-64-5 belongs to class bromides-buliding-blocks, and the molecular formula is C7H4BrNO4, Quality Control of 16426-64-5.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Smith, Alan’s team published research in Biochemical Journal in 1968 | 16426-64-5

Biochemical Journal published new progress about Nocardia. 16426-64-5 belongs to class bromides-buliding-blocks, and the molecular formula is C7H4BrNO4, Recommanded Product: 2-Bromo-4-nitrobenzoic acid.

Smith, Alan; Tranter, E. Karen; Cain, Ronald B. published the artcile< Utilization of some halogenated aromatic acids by Norcardia. Effects on growth and enzyme induction>, Recommanded Product: 2-Bromo-4-nitrobenzoic acid, the main research area is ENZYME INDUCTION NOCARDIA; HALOGENS ARYL NOCARDIA; NOCARDIA ARYL HALOGENS.

Halogen analogs of benzoate and p-nitrobenzoate did not support growth of N. erythropolis. These analogs, when present together with the parent compounds, inhibited growth of the organism. The halogen analogs similarly inhibited oxidation of benzoate or p-nitrobenzoate by competent cells. Fluoroacetate and 2-fluoro-4-nitrobenzoate caused comparable inhibition of growth on p-nitrobenzoate and both led to some citrate accumulation. The induction of the p-nitrobenzoate-oxidation system was strongly inhibited by all the 2-halogeno-4-nitrobenzoates although the 2-fluoro and 2-chloro derivatives also acted as inducers. Halogen analogs of benzoate also induced the benzoate-oxidation system.

Biochemical Journal published new progress about Nocardia. 16426-64-5 belongs to class bromides-buliding-blocks, and the molecular formula is C7H4BrNO4, Recommanded Product: 2-Bromo-4-nitrobenzoic acid.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Justoni, R’s team published research in Farmaco (1946-1952) in 1951 | 16426-64-5

Farmaco (1946-1952) published new progress about Dyes. 16426-64-5 belongs to class bromides-buliding-blocks, and the molecular formula is C7H4BrNO4, COA of Formula: C7H4BrNO4.

Justoni, R.; Pessina, R. published the artcile< Substances presumably with antitubercular action. I. Derivatives of 4-aminosalicylic acid acylated at the hydroxyl group>, COA of Formula: C7H4BrNO4, the main research area is .

Treating p-O2NC6H4Me with Br in the presence of Fe powder, washing with NaHSO3 solution, steam distillation, and crystallization from EtOH give 90% 2,4-Br(O2N)C6H3Me (I). Heat 5 kg. of I with 35 l. 65% HNO3 to the b.p. for 96 hrs., with 11.72% HNO3 added every 6 hrs., cool to -10°, sep. the acid liquid to treat another quantity of 5 kg. I, dilute the part in excess of 35 l., and distil to recover the unreacted I in the distillate and some of the Br(O2N)C6H3CO2H (II) in the residue; combine this residue with the bulk of II, dissolve in NH3, and precipitate with acid. The yield of II is 65%. II (2.46 kg.) in 4 l. H2O is mixed with 1 l. of 36° Bé. NaOH, heated 3 hrs. with 360 g. Cu(OAc)2 and 1.86 kg. Ba(OH)2.8H2O with further addition of 3 portions of 600 g. Ba(OH)2.8H2O, and the filtered paste of Ba p-nitrosalicylate treated with HCl to give the free acid (III). Acetylation gives 2,4-AcO(O2N)C6H3CO2H, m. 156°. Heating III with EtCOCl in PhMe gives 4,2-O2N(EtCO)C6H3CO2H, m. 153-4°. O-PrCO homolog, m. 134-5°; O-Me2CHCO homolog, m. 145-6°. The NO2 group is reduced at 20-5° with Pt black as a catalyst and the Me or Et ester of the acylated acid as solvent. 4,2-H2N(AcO)C6H3CO2H m. 136°. Further acetylation gives the N,O-di-Ac derivative, m. 189-90°. The O-EtCO acid m. 147°; O-PrCO acid m. 133°; O-Me2CHCO acid m. 150° (decomposition). Heating 2,4-HO(O2N)C6H3CO2Me with Ac2O gives 4,2-O2N(AcO)C6H3CO2Me, m. 79-80° (from petr. ether); iso-Pr ester, m. 44-5°. 4,2-O2N(AcO)C6H3CO2Me in 80% AcOH with Zn slowly forms 4,2-H2N(AcO)C6H3CO2Me, m. 109-10°; the O-EtCO homolog m. 111-12°. 4,2-H2N(AcO)C6H3CO2CHMe2 m. 141-2°; O-Me2CCO homolog m. 99-101°.

Farmaco (1946-1952) published new progress about Dyes. 16426-64-5 belongs to class bromides-buliding-blocks, and the molecular formula is C7H4BrNO4, COA of Formula: C7H4BrNO4.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary