돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1883017생성일: 2026년 10월 24일

Dihydro-3(2H)-thiophenone → 5-Chloro-N-(5-methylpyridin-2-yl)-2-{[1-(tetrahydrothiophen-3-yl)piperidin-4-yl]methylamino}benzamide

https://huagongshe.com/ko/reaction/1883017

반응식

참여 물질

역할이름HCID투입량
반응물Dihydro-3(2H)-thiophenoneHCID 61252—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물5-Chloro-N-(5-methylpyridin-2-yl)-2-[(4-piperidinylmethyl)amino]benzamideHCID 21906309—
용매TetrahydrofuranHCID 8028—
용매Acetic acid methanolHCID 10129899—
생성물5-Chloro-N-(5-methylpyridin-2-yl)-2-{[1-(tetrahydrothiophen-3-yl)piperidin-4-yl]methylamino}benzamideHCID 2190632177.3%

반응 조건

온도50 °C

반응 단계

A solution of 5-chloro-N-(5-methylpyridin-2-yl)-2-[(4-piperidinylmethyl)amino]benzamide from Example 99-A (0.45 g, 1.25 mmol) in 10 mL of 95:5 methanol-acetic acid was treated with excess tetrahydrothiophen-3-one (1.07 mL, 12.5 mmol), followed by sodium cyanoborohydride (5.0 ml of a 1 M solution in tetrahydrofuran, 6.0 mmol). After stirring at 50° C. for 96 h, the mixture was concentrated in vacuo; and the residue was subjected to silica gel chromatography. Elution with 9:1 dichloromethane-2 M ammonia in methanol afforded 0.43 g (77%) of the title compound as a yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06759414B2
출처 데이터셋uspto-grants-2004_07
ORD IDord-b4b22624256047f284aa275ed0a8c527
출처 메모uspto-grants-2004_07