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【结 构 式】

【分子编号】68448

【品名】2-bromo-3-nitrophenol

【CA登记号】101935-40-4

【 分 子 式 】C6H4BrNO3

【 分 子 量 】218.007

【元素组成】C 33.06% H 1.85% Br 36.65% N 6.42% O 22.02%

与该中间体有关的原料药合成路线共 1 条

合成路线1

该中间体在本合成路线中的序号:(XXVII)

Sandmeyer reaction of 2-amino-3-nitrophenol (XXVI) using NaNO2 and HBr in the presence of CuBr in H2O/dioxane gives 2-bromo-3-nitrophenol (XXVII), which by O-alkylation with MeI in the presence of Cs2CO3 in DMF affords the methyl ether (XXVIII). Subsequent reduction of the nitro derivative (XXVIII) with Fe powder in refluxing AcOH/EtOH provides 2-bromo-3-methoxyaniline (XXIX) . Addition of aniline (XXIX) to dimethyl acetylene dicarboxylate (XXX) in refluxing MeOH produces the amino diester (XXXI), which by cyclization at 240 °C in diphenyl ether affords the quinoline (X) .

1 Llinas-Brunet, M., Bailey, M.D., Goudreau, N. et al. Discovery of a potent and selective noncovalent linear inhibitor of the hepatitis C virus NS3 protease (BI 201335). J Med Chem 2010, 53(17): 6466-76.
2 Llinas-Brunet, M., Bailey, M., Bhardwaj, P. et al. (Boehringer Ingelheim International GmbH & Co. KG). Hepatitis C inhibitor compounds. US 7585845.
3 Bhardwaj, P., Forgione, P., Goudreau, N. et al. (Boehringer Ingelheim International GmbH). Hepatitis C inhibitor compounds. EP 1654261, JP 2006528937, JP 2010043129, US 2005020503, US 2011177030, US 8067438, WO 2004103996.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(X) 68434 methyl 8-bromo-4-hydroxy-7-methoxyquinoline-2-carboxylate   C12H10BrNO4 详情 详情
(XXVI) 41985 2-amino-3-nitrophenol 603-85-0 C6H6N2O3 详情 详情
(XXVII) 68448 2-bromo-3-nitrophenol 101935-40-4 C6H4BrNO3 详情 详情
(XXVIII) 68449 2-bromo-1-methoxy-3-nitrobenzene;2-Bromo-3-nitroanisole 67853-37-6 C7H6BrNO3 详情 详情
(XXIX) 68451 2-bromo-3-methoxyaniline   C7H8BrNO 详情 详情
(XXX) 24551 Dimethyl acetylenedicarboxylate; Dimethyl 2-butynedioate;Acetylenedicarboxylic acid dimethyl ester 762-42-5 C6H6O4 详情 详情
(XXXI) 68450 dimethyl 2-((2-bromo-3-methoxyphenyl)amino)maleate   C13H14BrNO5 详情 详情
Extended Information