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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 988679생성일: 2026년 10월 26일

Tetrahydrothiopyran-4-one → 5-Chloro-N-(5-methylpyridin-2-yl)-2-{[1-(tetrahydrothiopyran-4-yl)piperidin-4-yl]methyl-amino}benzamide

https://huagongshe.com/reaction/988679

반응식

참여 물질

역할이름HCID투입량
반응물Tetrahydrothiopyran-4-oneHCID 66173—
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-(tetrahydrothiopyran-4-yl)piperidin-4-yl]methyl-amino}benzamideHCID 2190656140.1%

반응 조건

온도50 °C

반응 단계

5-Chloro-N-(5-methylpyridin-2-yl)-2-[(4-piperidinylmethyl)amino]benzamide from Example 99-A (0.45 g, 1.25 mmol) was dissolved in 95:5 methanol-acetic acid (10 mL), followed by addition of tetrahydrothiopyran-4-one (1.46 g, 12.6 mmol) and 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 directly subjected to silica gel chromatography. Elution with 9:1 dichloromethane-methanol provided 0.23 g (40%) of the title product as a yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06635657B1
출처 데이터셋uspto-grants-2003_10
ORD IDord-bd380b5f06b94f91aac911c648f35ed9
출처 메모uspto-grants-2003_10