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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 437689생성일: 2026년 10월 24일

Dicyclohexylcarbodiimide → Nalphat-Butoxycarbonyl-L-tryptophyl-O-benzyl-D-seryl-O-benzyl-L-tyrosyl-D-alanine

https://huagongshe.com/ko/reaction/437689

반응식

참여 물질

역할이름HCID투입량
반응물DicyclohexylcarbodiimideHCID 10868—
반응물N-tert-Butoxycarbonyl-L-tryptophanHCID 83169—
반응물(R)-3-(benzyloxy)-2-((tert-butoxycarbonyl)amino)propanoic acidHCID 2733693—
반응물Nalpha-t-butoxycarbonyl-O-benzyl-L-tyrosyl-D-alanineHCID 12876484—
생성물Nalphat-Butoxycarbonyl-L-tryptophyl-O-benzyl-D-seryl-O-benzyl-L-tyrosyl-D-alanineHCID 86734883—

반응 조건

온도25 °C

반응 단계

Nαt-Butoxycarbonyl-L-tryptophyl-O-benzyl-D-seryl-O-benzyl-L-tyrosyl-D-alanine resin is prepared from 8 g. of Nα-t-butoxycarbonyl-O-benzyl-L-tyrosyl-D-alanine resin by successive coupling, according to the general process for solid phase synthesis given in Example 1, with (13 g., 9.8 mmol, of Nα-t-butoxycarbonyl-O-benzyl-D-serine and 2 g., 9.7 mmol, of dicyclohexylcarbodiimide and (2) 3 g., 9.8 mmol, of Nα-t-butoxycarbonyl-L-tryptophan and 2 g. of dicyclohexylcarbodiimide. The resin is washed with ethanol and dried. It is then stirred for twenty-four hours at 25° C. with 200 ml. of methanol and 20 ml. of triethylamine. The mixture is filtered and the methanol solution evaporated. The residue is solidified from ether-petroleum ether; 2 g.; m.p. 155°-156° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04031069
출처 데이터셋uspto-grants-1977_06
ORD IDord-7e5c7cd0664f4808bd5f2344c1495cfb
출처 메모uspto-grants-1977_06