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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 415306생성일: 2026년 10월 24일

benzyl 3-(chlorocarbonyl)tetrahydro-1(2H)-pyridinecarboxylate → Benzyl-3-(2-hydroxy-3-(methoxycarbonyl)phenylcarbamoyl)piperidine-1-carboxylate

https://huagongshe.com/ko/reaction/415306

반응식

참여 물질

역할이름HCID투입량
반응물benzyl 3-(chlorocarbonyl)tetrahydro-1(2H)-pyridinecarboxylateHCID 2776575—
반응물Methyl 3-amino-2-hydroxybenzoateHCID 12782444—
용매DichloromethaneHCID 6344—
생성물Benzyl-3-(2-hydroxy-3-(methoxycarbonyl)phenylcarbamoyl)piperidine-1-carboxylateHCID 6662133197%

반응 단계

Benzyl 3-(chlorocarbonyl)piperidine-1-carboxylate (500 mg, 3 mmol) and methyl 3-amino-2-hydroxybenzoate (1.014 g, 3.6 mmol) were added in anhydrous dichloromethane (20 mL) and the mixture was stirred at room temperature overnight. The mixture was extracted with dichloromethane (100 mL×4) and the organic phase was dried with anhydrous sodium sulfate and evaporated under reduced pressure. 1.2 g benzyl-3-(2-hydroxy-3-(methoxycarbonyl)phenylcarbamoyl)piperidine-1-carboxylate was obtained. Yield: 97%. LC-MS (ESI) m/z: 413 (M+1)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08088760B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-3803e9b9c49f4cbc82b19b5be917c2cc
출처 메모uspto-grants-2012_01