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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Dihydro-3(2H)-thiophenone | HCID 61252 | — |
| 반응물 | Sodium cyanoborohydride | HCID 5003444 | — |
| 반응물 | 5-Chloro-N-(5-methylpyridin-2-yl)-2-[(4-piperidinylmethyl)amino]benzamide | HCID 21906309 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Acetic acid methanol | HCID 10129899 | — |
| 생성물 | 5-Chloro-N-(5-methylpyridin-2-yl)-2-{[1-(tetrahydrothiophen-3-yl)piperidin-4-yl]methylamino}benzamide | HCID 21906321 | 77.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06759414B2 |
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| 출처 데이터셋 | uspto-grants-2004_07 |
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| ORD ID | ord-b4b22624256047f284aa275ed0a8c527 |
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| 출처 메모 | uspto-grants-2004_07 |
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