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HRID 1894468生成日期:2026年10月23日

3-氨基-2,6-二甲基吡啶 → 2-{4-[(4S,5R)-2-(6-tert-Butyl-4-ethoxy-pyridin-3-yl)-4,5-bis-(4-chloro-phenyl)-4,5-dimethyl-4,5-dihydro-imidazole-1-carbonyl]-piperazin-1-yl}-N-(2,6-dimethyl-pyridin-3-yl)-acetamide

https://huagongshe.com/zh-CN/reaction/1894468

反应方程式

参与物

角色名称HCID投料
反应物3-氨基-2,6-二甲基吡啶HCID 76964—
反应物{4-[(4S,5R)-2-(6-tert-Butyl-4-ethoxy-pyridin-3-yl)-4,5-bis-(4-chloro-phenyl)-4,5-dimethyl-4,5-dihydro-imidazole-1-carbonyl]-piperazin-1-yl}-acetic acid hydrochlorideHCID 25262898—
产物2-{4-[(4S,5R)-2-(6-tert-Butyl-4-ethoxy-pyridin-3-yl)-4,5-bis-(4-chloro-phenyl)-4,5-dimethyl-4,5-dihydro-imidazole-1-carbonyl]-piperazin-1-yl}-N-(2,6-dimethyl-pyridin-3-yl)-acetamideHCID 57670014—

反应步骤

In a manner analogous to the method described in examples 99, {4-[(4S,5R)-2-(6-tert-butyl-4-ethoxy-pyridin-3-yl)-4,5-bis-(4-chloro-phenyl)-4,5-dimethyl-4,5-dihydro-imidazole-1-carbonyl]-piperazin-1-yl}-acetic acid hydrochloride (example 94) was coupled with 2,6-dimethyl-pyridin-3-ylamine (Alfa) to give the title compound. HR-MS (ES, m/z) calculated for C42H50Cl2N7O3 [(M+H)+] 770.3347, observed 770.3351.

来源与证据

DOI10.6084/m9.figshare.5104873.v1
专利号US08513239B2
来源数据集uspto-grants-2013_08
ORD IDord-e686bfce76a843a28848cd39cd3063b5
来源说明uspto-grants-2013_08