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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4983생성일: 2026년 10월 23일

N-(tert-butoxycarbonyl)glycine → Boc-Gly-Leu-Ala-OBzl

https://huagongshe.com/ko/reaction/4983

반응식

참여 물질

역할이름HCID투입량
반응물N-(tert-butoxycarbonyl)glycineHCID 78288—
반응물H-Leu-Ala-OBzlHCID 16742166—
생성물Boc-Gly-Leu-Ala-OBzlHCID 131717744—

반응 단계

Boc-Gly-Leu-Ala-OBzl was prepared by coupling Boc-Gly-OH (5.70 g, 32.6 mmoles) to H-Leu-Ala-OBzl using the mixed anhydride procedure described in Example 2. The product (13.8 g) was obtained as an amorphous solid. Boc-Gly-Leu-Ala-OBzl was deblocked with trifluoroacetic acid by the procedure described for the preparation of H-Leu-Ala-OBzl except that the trifluoroacetate salt was soluble in ether. The preparation was dissolved in ethyl acetate and treated with anhydrous hydrogen chloride. The resulting product was precipitated by the addition of ether to yield 7.7 g of H-Gly-Leu-Ala-OBzl HCl in a first crop.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05242904
출처 데이터셋uspto-grants-1993_09
ORD IDord-e95bb68602144d5c8b548570c446fb1d
출처 메모uspto-grants-1993_09