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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 221369생성일: 2026년 10월 25일

Cyclopentyl chloroformate → 4-[Methyl-(3-pyridin-4-yl-[1,2,4]oxadiazol-5-ylmethyl)amino]piperidine-1-carboxylic acid cyclopentyl ester

https://huagongshe.com/reaction/221369

반응식

참여 물질

역할이름HCID투입량
반응물Cyclopentyl chloroformateHCID 2735892—
반응물Methylpiperidin-4-yl-(3-pyridin-4-yl-[1,2,4]oxadiazol-5-ylmethyl)amineHCID 69078503—
생성물4-[Methyl-(3-pyridin-4-yl-[1,2,4]oxadiazol-5-ylmethyl)amino]piperidine-1-carboxylic acid cyclopentyl esterHCID 57954401—

반응 단계

The tert-butoxycarbonyl group of 4-[methyl(3-pyridin-4-yl-[1,2,4]oxadiazol-5-ylmethyl)amino]piperidine-1-carboxylic acid tert-butyl ester (Example 119) was removed using the procedure described in Example 51 to afford methylpiperidin-4-yl-(3-pyridin-4-yl-[1,2,4]oxadiazol-5-ylmethyl)amine: RT=0.65 min; m/z (ES+)=274.0 [M+H]+. Derivatisation of methylpiperidin-4-yl-(3-pyridin-4-yl-[1,2,4]oxadiazol-5-ylmethyl)amine with cyclopentylchloroformate, using the procedure described for Example 52, afforded the title compound: RT=3.02 min; m/z (ES+)=386.0 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08207147B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-a00f6c714b644589a6684cae9d2104fc
출처 메모uspto-grants-2012_06