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【结 构 式】

【分子编号】26792

【品名】N-[3-amino-2-(2-bromo-4-isopropylanilino)-6-methyl-4-pyridinyl]-N-butyl-N-ethylamine

【CA登记号】

【 分 子 式 】C21H31BrN4

【 分 子 量 】419.4081

【元素组成】C 60.14% H 7.45% Br 19.05% N 13.36%

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:(VIII)

4-Hydroxy-6-methyl-3-nitro-2-pyridone (I) was treated with phosphoryl chloride in boiling N,N-diethylaniline, and the resulting dichloropyridine (II) was condensed with n-butyl ethylamine (III) to afford a regioisomeric mixture of 4- (IV) and 2-amino (V) pyridines. After chromatographic separation, the desired isomer (IV) was coupled with 2-bromo-4-isopropylaniline (VI) at 140 C to provide (VII). Reduction of the nitro group of (VII) using sodium hydrosulfite and ammonia yielded diamine (VIII). Subsequent cyclization of (VIII) with phosgene in refluxing toluene gave imidazopyridinone (IX), which was finally N-methylated by means of CH3I and KOH in acetone.

1 Beck, J.P.; et al.; Purin-8-ones as corticotropin-releasing hormone (CRH-R1) receptor antagonists. Bioorg Med Chem Lett 1999, 9, 7, 967.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(I) 23337 4-hydroxy-6-methyl-3-nitro-2(1H)-pyridinone 4966-90-9 C6H6N2O4 详情 详情
(II) 26787 2,4-dichloro-6-methyl-3-nitropyridine C6H4Cl2N2O2 详情 详情
(III) 26788 N-butyl-N-ethylamine 13360-63-9 C6H15N 详情 详情
(IV) 26789 N-butyl-2-chloro-N-ethyl-6-methyl-3-nitro-4-pyridinamine C12H18ClN3O2 详情 详情
(V) 26790 N-butyl-4-chloro-N-ethyl-6-methyl-3-nitro-2-pyridinamine C12H18ClN3O2 详情 详情
(VI) 23782 2-bromo-4-isopropylaniline; 2-bromo-4-isopropylphenylamine 51605-97-1 C9H12BrN 详情 详情
(VII) 26791 N-[2-(2-bromo-4-isopropylanilino)-6-methyl-3-nitro-4-pyridinyl]-N-butyl-N-ethylamine C21H29BrN4O2 详情 详情
(VIII) 26792 N-[3-amino-2-(2-bromo-4-isopropylanilino)-6-methyl-4-pyridinyl]-N-butyl-N-ethylamine C21H31BrN4 详情 详情
(IX) 26793 3-(2-bromo-4-isopropylphenyl)-7-[butyl(ethyl)amino]-5-methyl-1,3-dihydro-2H-imidazo[4,5-b]pyridin-2-one C22H29BrN4O 详情 详情
Extended Information