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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 253598생성일: 2026년 10월 26일

Triethylamine → 3-((2S,3R)-4-(N-(4-Cyanobenzyl)-N-(2-(trimethylsilyl)ethoxycarbonyl)amino)-1-cyclohexyl-3-hydroxybutan-2-ylamino)-4-methoxycyclobut-3-ene-1,2-dione

https://huagongshe.com/reaction/253598

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물3-Cyclobutene-1,2-dione, 3,4-dimethoxy-HCID 123227—
반응물HCID 66861734HCID 66861734—
용매EthanolHCID 702—
생성물3-((2S,3R)-4-(N-(4-Cyanobenzyl)-N-(2-(trimethylsilyl)ethoxycarbonyl)amino)-1-cyclohexyl-3-hydroxybutan-2-ylamino)-4-methoxycyclobut-3-ene-1,2-dioneHCID 86632800—

반응 단계

A solution of (2R,3S)-1-(N-(4-cyanobenzyl)-N-(2-(trimethylsilyl)ethoxycarbonyl)amino)-2-hydroxy-3-amino-4-cyclohexylbutane (764 mg, 1.68 mmol) in EtOH (20 mL) was treated with 3,4-dimethoxycyclobut-3-ene-1,2-dione (300 mg, 2.10 mmol, 1.25 equiv) and Et3N (212 mg, 1.25 equiv). The resulting solution was allowed to stir at rt for 17 h. The excess 3,4-dimethoxycyclobut-3-ene-1,2-dione was removed by flash chromatography on silica gel, eluting with 0-65% EtOAc in hexanes. Analysis of the compound by LC-MS showed that it was of sufficient purity to employ in the subsequent steps.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07872028B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-f3a06eccc2fa4bc788578fc76fb70eb3
출처 메모uspto-grants-2011_01