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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 29743생성일: 2026년 10월 26일

Diisopropylethylamine → 2-[(1-Benzyloxycarbonylamino-2-methylpropyl)-methoxy-phosphinoyloxy]-5-tert-butoxycarbonylamino-pentanoic acid methyl ester

https://huagongshe.com/reaction/29743

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물PyBOPHCID 2724699—
반응물(1-Benzyloxycarbonylamino-2-methyl-propyl)-phosphonic acid monomethyl esterHCID 10380108—
반응물5-Tert-butoxycarbonylamino-2-hydroxy-pentanoic acid methyl esterHCID 54330025—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물2-[(1-Benzyloxycarbonylamino-2-methylpropyl)-methoxy-phosphinoyloxy]-5-tert-butoxycarbonylamino-pentanoic acid methyl esterHCID 5439201869%

반응 단계

A solution of PyBOP (2.1 g, 4.0 mmol) in DMF (3 mL) was added to a mixture of (1-benzyloxycarbonylamino-2-methyl-propyl)-phosphonic acid monomethyl ester (1.0 g, 3.32 mmol) and 5-tert-butoxycarbonylamino-2-hydroxy-pentanoic acid methyl ester (865 mg, 3.5 mmol) in DMF (4 mL) under argon. DIPEA (2.28 mL, 13.3 mmol) was added dropwise and the mixture was stirred over night. Ethyl acetate was added and the mixture was washed with 10% KHSO4, satd. NaHCO3 and brine and dried. Concentration under reduced pressure followed by chromathography (heptane/EtOAc, 1:1→1:6) gave 2-[(1-benzyloxycarbonylamino-2-methyl-propyl)-methoxy-phosphinoyloxy]-5-tert-butoxycarbonylamino-pentanoic acid methyl ester (1.21 g, 69%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07423012B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-b6f4d112812d4f00b22a247b00911401
출처 메모uspto-grants-2008_09