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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 393442생성일: 2026년 10월 25일

Diisopropylethylamine → 4-[[(4-cyano-4-phenyl-1-piperidinyl)carbonyl]amino]-N-[(2,2-dichloro-1-methylcyclopropyl)carbonyl]-L-phenylalanine

https://huagongshe.com/reaction/393442

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물2,2-Dichloro-1-methylcyclopropanecarboxylic acidHCID 102621—
반응물Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
반응물4-[[(4-cyano-4-phenyl-1-piperidinyl)carbonyl]amino]-L-phenylalanineHCID 53977714—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물4-[[(4-cyano-4-phenyl-1-piperidinyl)carbonyl]amino]-N-[(2,2-dichloro-1-methylcyclopropyl)carbonyl]-L-phenylalanineHCID 57125853—

반응 단계

A suspension of 4-[[(4-cyano-4-phenyl-1-piperidinyl)carbonyl]amino]-L-phenylalanine on Wang resin (0.30 g, 0.228 mmol), 2,2-dichloro-1-methylcyclopropane carboxylic acid (0.19 g, 1.14 mmol), BOP (0.50 g, 1.14 mmol) and DIPEA (0.26 mL, 1.5 mmol) in N-methylpyrrolidinone (3 mL) was agitated for 3 hr. The mixture was filtered and washed with dichloromethane and methanol. Cleavage from the resin was effected by treatment with 90% TFA in dichloromethane for 3 min. The mixture was filtered and the filtrate evaporated to give 4-[[(4-cyano-4-phenyl-1-piperidinyl)carbonyl]amino]-N-[(2,2-dichloro-1-methylcyclopropyl)carbonyl]-L-phenylalanine. FAB MS m/z 543 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06806365B2
출처 데이터셋uspto-grants-2004_10
ORD IDord-f7012c36992b49ada743a4b148da1dc5
출처 메모uspto-grants-2004_10