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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1894415생성일: 2026년 10월 23일

Thiomorpholine 1,1-dioxide → 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}-1-(1,1-dioxo-1lambda6-thiomorpholin-4-yl)-ethanone

https://huagongshe.com/ko/reaction/1894415

반응식

참여 물질

역할이름HCID투입량
반응물Thiomorpholine 1,1-dioxideHCID 6484228—
반응물{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—
생성물2-{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}-1-(1,1-dioxo-1lambda6-thiomorpholin-4-yl)-ethanoneHCID 25262737—

반응 단계

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 thiomorpholine 1,1-dioxide (Syntech Development) to give the title compound. HR-MS (ES, m/z) calculated for C39H49Cl2N6O5S [(M+H)+] 783.2857, observed 783.2856.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08513239B2
출처 데이터셋uspto-grants-2013_08
ORD IDord-2f18a2545cbe49f585cbf8f5dc6c2c07
출처 메모uspto-grants-2013_08