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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 614205생성일: 2026년 10월 25일

4-Methylmorpholine → N-t-butoxycarbonyl-L-tyrosyl-glycylglycyl-L-phenylalanyl-L-methionine sulfoxide

https://huagongshe.com/reaction/614205

반응식

참여 물질

역할이름HCID투입량
반응물4-MethylmorpholineHCID 7972—
반응물Isobutyl chloroformateHCID 62365—
반응물Methionine SulfoxideHCID 158980—
반응물N-t-butoxycarbonyl-L-tyrosylglycylglycyl-L-phenylalanineHCID 15689707—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물N-t-butoxycarbonyl-L-tyrosyl-glycylglycyl-L-phenylalanyl-L-methionine sulfoxideHCID 22807105—

반응 조건

온도-15 °C

반응 단계

10.84 Parts N-t-butoxycarbonyl-L-tyrosylglycylglycyl-L-phenylalanine and 2.0 parts N-methylmorpholine are dissolved in 200 parts dimethylformamide and cooled to -15° C. Then, 2.9 parts isobutyl chloroformate is added dropwise over a thirty minute period while keeping the temperature between -15° C. to -10° C. After the addition is completed, a solution of 3.3 parts L-methionine sulfoxide in 15 parts dimethylformamide is slowly added. The mixture is stirred for a further thirty minutes at -15° C. and then warmed to room temperature and stirred thereat for an additional 2 hours. The product is isolated by diluting the reaction mixture with 10 volumes water and extracting with ethyl acetate. The ethyl acetate extracts are combined, dried over anhydrous sodium sulfate and stripped of solvent under reduced pressure. The residue is purified by low-pressure chromatography to afford N-t-butoxycarbonyl-L-tyrosyl-glycylglycyl-L-phenylalanyl-L-methionine sulfoxide.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04144228
출처 데이터셋uspto-grants-1979_03
ORD IDord-e84d01dcc5bb477a9e3f431693996d68
출처 메모uspto-grants-1979_03