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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 429522생성일: 2026년 10월 25일

Hydrogen Bromide → 1-[2(R)-[1(R)-carboxy-2-(3,4,4-trimethyl-2,5-dioxo-1-imidazolidinyl)ethyl]-3-cyclopentylpropionyl)piperdine

https://huagongshe.com/reaction/429522

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen BromideHCID 260—
반응물1-[2(R)-[1(S)-(tert-butoxycarbonyl)-2-(3,4,4-trimethyl-2,5-dioxo-1imidazolidinyl)ethyl]-3-cyclopentylpropionyl]piperidineHCID 23382264—
용매Acetic AcidHCID 176—
용매DichloromethaneHCID 6344—
생성물1-[2(R)-[1(R)-carboxy-2-(3,4,4-trimethyl-2,5-dioxo-1-imidazolidinyl)ethyl]-3-cyclopentylpropionyl)piperdineHCID 11270129—

반응 단계

A solution of 15.11 g of the 9:1 mixture from Example 4 in 15 ml of acetic acid was treated at 0° with 15 ml of 33% hydrogen bromide in acetic acid and stirred at 0° for 4 hrs. The solution was diluted with methylene chloride, washed with water and the organic phase was dried, filtered and evaporated. The residue was crystallized from 26 ml of tert-butyl methyl ether and 26 ml of hexane, after which 6.90 g (70%) of diastereomer-pure (de >98%) 1-[2(R)-[1(R)-carboxy-2-(3,4,4,-trimethyl-2,5-dioxo-1-imidazolidinyl)ethyl]-3-cyclopentylpropionyl]piperidine (IX), m.p. 111-114°, was obtained. IR (KBr): 1770m and 1715s (C═O).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06316633B1
출처 데이터셋uspto-grants-2001_11
ORD IDord-bc344bec804e42dbbbd37f3b47c6b3e7
출처 메모uspto-grants-2001_11