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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 8747생성일: 2026년 10월 23일

Trimethylsilyldiazomethane → Methyl 4-(1-(tert-butoxycarbonyl)-4-(methoxycarbonyl)piperidin-4-yl)butanoate

https://huagongshe.com/ko/reaction/8747

반응식

참여 물질

역할이름HCID투입량
반응물TrimethylsilyldiazomethaneHCID 167693—
반응물4-(1-(tert-Butoxycarbonyl)-4-(methoxycarbonyl)piperidin-4-yl)butanoic acidHCID 21983987—
용매Dichloromethane methanolHCID 21226129—
생성물Methyl 4-(1-(tert-butoxycarbonyl)-4-(methoxycarbonyl)piperidin-4-yl)butanoateHCID 6918385082.4%

반응 단계

To a solution of 4-(1-(tert-butoxycarbonyl)-4-(methoxy-carbonyl)piperidin-4-yl)butanoic acid (23.4 g, 0.071 mol) from Step D in 3:1 dichloromethane/methanol (480 mL) at 0° C. was added a solution of trimethylsilyldiazomethane (53 mL, 0.11 mol, 2.0M in hexane). The reaction mixture was stirred for 15 min and then concentrated to afford 25.5 g. The residue was purified by flash chromatography eluting with 20–30% ethyl acetate in hexanes to give the title compound (20.1 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091211B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-6b2aefe82fc74fb8a87e403b637a98cc
출처 메모uspto-grants-2006_08