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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1915963생성일: 2026년 10월 26일

Diethylamine → (R)-4-(9H-Fluoren-9-ylmethoxycarbonylamino)-4-{(S)-1-[1-(1-hydroxy-2-methoxycarbonyl-ethyl)-cyclopropylcarbamoyl]-2-tritylsulfanyl-ethylcarbamoyl}-butyric acid tert-butyl ester

https://huagongshe.com/reaction/1915963

반응식

참여 물질

역할이름HCID투입량
반응물DiethylamineHCID 8021—
반응물DiisopropylethylamineHCID 81531—
반응물PyBOPHCID 2724699—
반응물(2R)-5-(tert-butoxy)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-5-oxopentanoic acidHCID 7018822—
반응물3-{1-[(s)-2-(9h-Fluoren-9-ylmethoxycarbonylamino)-3-tritylsulfanyl-propionylamino]-cyclopropyl}-3-hydroxy-propionic acid methyl esterHCID 67022418—
용매AcetonitrileHCID 6342—
용매DichloromethaneHCID 6344—
생성물(R)-4-(9H-Fluoren-9-ylmethoxycarbonylamino)-4-{(S)-1-[1-(1-hydroxy-2-methoxycarbonyl-ethyl)-cyclopropylcarbamoyl]-2-tritylsulfanyl-ethylcarbamoyl}-butyric acid tert-butyl esterHCID 8728976194%

반응 단계

To 4 (908 mg, 1.28 mmol) in MeCN (10 mL) was added diethylamine (1 mL, 10% v/v), and the reaction mixture was stirred for 2 h. The mixture was then concentrated in vacuo, MeCN (3×20 mL) was added, then removed in vacuo, and the crude amine was placed under high vacuum for 2 h. Subsequently, to a solution of PyBOP (705 mg, 1.35 mmol) and Fmoc-D-Glu(OtBu)-OH (577.8 mg, 1.36 mmol) in CH2Cl2 (15 mL) at 0° C. was added diisopropylethylamine (0.70 mL, 4.02 mmol) under Ar(g) and the mixture was stirred for 2 min. A solution of the crude amine derivative of 4 in MeCN (15 mL) was added, and the mixture was stirred at rt for 16 h, and the solvent was then removed in vacuo. Purification by flash column chromatography on silica (eluant 4:6-6:4 EtOAc/Hexane) gave 5 (1.099 g, 1.20 mmol, 94%) as a white solid: Rf 0.54 EtOAc/Hexane (6:4), and as a mixture of diastereoisomers not resolved by 1H NMR.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08614193B2
출처 데이터셋uspto-grants-2013_12
ORD IDord-862f2a85e76c4c308d77f45d8b820332
출처 메모uspto-grants-2013_12