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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 394045생성일: 2026년 10월 24일

tert-Butyl 3-(aminomethyl)pyrrolidine-1-carboxylate → (2R)-1-{(2S,4R)-4-hydroxy-1-(3,3,3-triphenylpropanoyl)pyrrolidin-2-yl}carbonyl-N-(3-pyrrolidylmethyl)pyrrolidine-2-carboxamide

https://huagongshe.com/ko/reaction/394045

반응식

참여 물질

역할이름HCID투입량
반응물tert-Butyl 3-(aminomethyl)pyrrolidine-1-carboxylateHCID 2756485—
반응물(1-Benzylpyrrolidin-3-yl)methanolHCID 5176654—
반응물(2R)-1-{(2S,4R)-4-(tert-butoxy)-1-(3,3,3-triphenylpropanoyl)pyrrolidin-2-yl}carbonylpyrrolidine-2-carboxylic acidHCID 69100730—
생성물(2R)-1-{(2S,4R)-4-hydroxy-1-(3,3,3-triphenylpropanoyl)pyrrolidin-2-yl}carbonyl-N-(3-pyrrolidylmethyl)pyrrolidine-2-carboxamideHCID 69101451—

반응 단계

The title compound was prepared by successively conducting procedures similar to Step 5 of Example 1 and Example 46, using 3-aminomethyl-1-(t-butoxycarbonyl)pyrrolidine [which was synthesized by a method similar to the one described in Japan Kokai Hei 11(1999)-193232, using 3-hydroxymethyl-1-benzylpyrrolidine [taught in Japan Kokai (laid-open) Hei 4(1992)-112868]] and (2R)-1-{(2S,4R)-4-(tert-butoxy)-1-(3,3,3-triphenylpropanoyl)pyrrolidin-2-yl}carbonyl-pyrrolidine-2-carboxylic acid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06809108B1
출처 데이터셋uspto-grants-2004_10
ORD IDord-bec0cd5890bc44568b80a3f430664f9c
출처 메모uspto-grants-2004_10