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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 989574생성일: 2026년 10월 24일

4-Methylmorpholine → Trt-Gly-Gly-Phe-Gly-OBz

https://huagongshe.com/ko/reaction/989574

반응식

참여 물질

역할이름HCID투입량
반응물4-MethylmorpholineHCID 7972—
반응물DicyclohexylcarbodiimideHCID 10868—
반응물N-HydroxysuccinimideHCID 80170—
반응물N-(Triphenylmethyl)glycylglycineHCID 14217166—
반응물Phe-Gly-OBzlHCID 91977316—
용매DimethylformamideHCID 6228—
생성물Trt-Gly-Gly-Phe-Gly-OBzHCID 131723527—

반응 단계

To 10 ml of dry DMF were added 1.54 g of Trt-Gly-Gly, 0.52 g of N-hydroxysuccinimide and 0.93 g of DCC, followed by effecting a reaction at 4° C. for 3 hours, to thereby obtain a reaction mixture. To the obtained reaction mixture was added a DMF solution containing 2.0 g of Phe-Gly-OBn para-toluenesulfonate synthesized in item (1) and 0.41 g of N-methylmorpholine, which are dissolved in 10 ml of DMF, followed by effecting a reaction at 4° C. for 15 hours, to thereby obtain a reaction mixture. A precipitate contained in the obtained reaction mixture was removed and the resultant solution was evaporated to dryness, to thereby obtain a residue. The obtained residue was purified by silica gel column chromatography (silica gel: Art No. 9365, Silica gel 60, 200-400 mesh, manufactured and sold by E. Merck, Darmstadt, Germany, eluent: chloroform/methanol=20/1), to thereby obtain 1.5 g of Trt-Gly-Gly-Phe-Gly-OBz.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06458347B1
출처 데이터셋uspto-grants-2002_10
ORD IDord-ad867d2c90d8478fa63c44df7dbe56a8
출처 메모uspto-grants-2002_10