돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 742991생성일: 2026년 10월 23일

Fmoc-L-tryptophan → N-(Fmoc-L-tryptophanyl)-1-amino-3-methylbutane

https://huagongshe.com/ko/reaction/742991

반응식

참여 물질

역할이름HCID투입량
반응물Fmoc-L-tryptophanHCID 978343—
용매IsoamylamineHCID 7894—
생성물N-(Fmoc-L-tryptophanyl)-1-amino-3-methylbutaneHCID 22865445196.3%

반응 단계

In substantially the same manner as in Example 5, 1-amino-3-methylbutane (405 μl) was condensed with Fmoc-Trp-OH (1.35 g, Peptide Institute, Inc.) to give N-(Fmoc-L-tryptophanyl)-1-amino-3-methylbutane (1.54 g) as a white powder (yield 98%). A portion (1.44 g) of this product was, in substantially the same manner as in Example 17, subjected to deprotection of Fmoc group, which was then condensed with (2S,3S)-ethyl hydrogen transepoxysuccinate as obtained in Reference Example 8 (432 mg) to yield the title compound (compound 88; 734 mg) as a white powder (yield 72%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05556853
출처 데이터셋uspto-grants-1996_09
ORD IDord-0e88a5bef1f54ec596166234daa51ec2
출처 메모uspto-grants-1996_09