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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 324595생성일: 2026년 10월 24일

Tricyclo(3.3.1.1'3,7)dec-1-ylmethanol → tert-Butyl (2S)-(adamant-1-ylmethoxycarbonylamino)-3-tert-butoxycarbonylaminopropionate

https://huagongshe.com/ko/reaction/324595

반응식

참여 물질

역할이름HCID투입량
반응물Tricyclo(3.3.1.1'3,7)dec-1-ylmethanolHCID 64556—
반응물1,1'-CarbonyldiimidazoleHCID 68263—
반응물DiisopropylethylamineHCID 81531—
반응물(S)-tert-Butyl 2-amino-3-((tert-butoxycarbonyl)amino)propanoate hydrochlorideHCID 86585733—
용매TetrahydrofuranHCID 8028—
생성물tert-Butyl (2S)-(adamant-1-ylmethoxycarbonylamino)-3-tert-butoxycarbonylaminopropionateHCID 68828668—

반응 조건

온도60 °C

반응 단계

A solution of 10.9 g (65.4 mmol) of (1-hydroxymethyl)adamantane and 10.6 g (65.4 mmol) of carbonyldiimidazole in 60 ml of THF is stirred at 50° C. for 1.5 h. 9.7 g (32.7 mmol) of (13.9) in 25 ml of THF and 5.6 ml (32.7 mmol) of diisopropylethylamine (DIPEA) are added and the mixture is stirred at 60° C. for 4 h and then left to stand at room temperature overnight. The solvent is removed in vacuo and the residue is chromatographed through silica gel using heptane/ethyl acetate=7/3. 8.7 9 (59%) of (13.10) are obtained as a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06218415B1
출처 데이터셋uspto-grants-2001_04
ORD IDord-792933421eae4e7fbca11c9b232f95ea
출처 메모uspto-grants-2001_04