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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 479617생성일: 2026년 10월 26일

Diisopropylethylamine → tert-butyl(3R)-6-cyclohexyl-3-({[(1S)-2-ethoxy-1-(hydroxymethyl)-2-oxoethyl]amino}carbonyl)hexanoate

https://huagongshe.com/reaction/479617

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참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물L-Serine, ethyl ester, hydrochloride (1:1)HCID 2724185—
반응물1-Hydroxybenzotriazole hydrateHCID 2796029—
반응물(2R)-2-[2-(tert-butoxy)-2-oxoethyl]-5-cyclohexylpentanoic acidHCID 9835906—
용매DichloromethaneHCID 6344—
생성물tert-butyl(3R)-6-cyclohexyl-3-({[(1S)-2-ethoxy-1-(hydroxymethyl)-2-oxoethyl]amino}carbonyl)hexanoateHCID 5990982478.1%

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온도0 °C

반응 단계

A solution of (2R)-2-[2-(tert-butoxy)-2-oxoethyl]-5-cyclohexylpentanoic acid (Preparation 25) (5.00 g, 16.76 mmol) in dichloromethane (75 ml) was treated sequentially with 1-hydroxybenzotriazole hydrate (2.49 g, 18.43 mmol), serine ethyl ester hydrochloride (3.13 g, 18.43 mmol) and N,N-diisopropylethylamine (6.13 ml, 35.19 mmol) and the resulting mixture was stirred at 0° C. under a nitrogen atmosphere for 15 minutes. 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride (3.53 g, 18.43 mmol) was then added and the mixture was stirred for 48 hours being allowed to warm to room temperature over this time. The mixture was diluted with dichloromethane (200 ml), washed sequentially with water, aqueous citric acid solution (10% w/v), a saturated aqueous solution of sodium hydrogen carbonate and brine, dried over anhydrous magnesium sulphate, filtered and the solvent removed under reduced pressure. The residue was then purified by column chromatography on silica gel eluting a gradient system of ethyl acetate:pentane (10:90) to (50:50) to afford the title compound as a colourless oil (5.41 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06645993B2
출처 데이터셋uspto-grants-2003_11
ORD IDord-2f227e70b476456ab8d77aa47c0ccebd
출처 메모uspto-grants-2003_11