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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 132700생성일: 2026년 10월 27일

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → (1S,5S)-(1-{5-[(4-amino-benzenesulfonyl)-isobutyl-amino]-6-phosphonooxy hexylcarbamoyl}-2,2-diphenyl-ethyl)-carbamic acid methyl ester

https://huagongshe.com/reaction/132700

반응식

참여 물질

역할이름HCID투입량
반응물1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물(S)-2-methoxycarbonylamino-3,3-diphenyl-propionic acidHCID 10017620—
반응물(2S)-phosphoric acid 6-amino-2-[(4-amino-benzenesulfonyl)-isobutyl-amino]-hexyl ester diethyl esterHCID 59733921—
용매DimethylformamideHCID 6228—
생성물(1S,5S)-(1-{5-[(4-amino-benzenesulfonyl)-isobutyl-amino]-6-phosphonooxy hexylcarbamoyl}-2,2-diphenyl-ethyl)-carbamic acid methyl esterHCID 11563875139.6%

반응 단계

(2S)-2-methoxycarbonylamino-3,3-diphenyl-propionic acid ((example 1, step E) 0.9 g, 3 mmol) was activated in DMF (5 mL) with EDAC (1.7 g, 9 mmol) and HOBt (1.2 g, 9 mmol). To the solution was added 1.17 g of (2S)-phosphoric acid 6-amino-2-[(4-amino -benzenesulfonyl)-isobutyl-amino]-hexyl ester diethyl ester (1X) (example 3, step B) and the mixture stirred for 3 h. 20 g of Amberlite XAD-2 resin was then added and the beads were left to soak for 10 min. The resin was transferred into a glass filter and washed thoroughly with distilled water (400 mL) and 200 mL of 1M NaHCO3. The beads were then washed with 4×50 ml portions of MeOH then EtOAc 200 mL. The organic phase was evaporated. The residue was adsorbed onto silica gel and passed through a short silica gel column (EtOAc) to yield 2.4 g (83%) of white solid after evaporation.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07388008B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-3e86046866034a439a328c075f181b75
출처 메모uspto-grants-2008_06