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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 3787생성일: 2026년 10월 23일

t-butoxycarbonyl-D-methionylglycyl-N-(6-methoxy-6-oxohexyl)-L-phenylalaninamide → D-methionylglycyl-N-(6-methoxy-6-oxohexyl)-L-phenylalaninamide monohydrochloride hemihydrate

https://huagongshe.com/ko/reaction/3787

반응식

참여 물질

역할이름HCID투입량
반응물t-butoxycarbonyl-D-methionylglycyl-N-(6-methoxy-6-oxohexyl)-L-phenylalaninamideHCID 13385843—
반응물1,4-Dioxane hydrochlorideHCID 20443148—
용매1,4-DioxaneHCID 31275—
생성물D-methionylglycyl-N-(6-methoxy-6-oxohexyl)-L-phenylalaninamide monohydrochloride hemihydrateHCID 131714086—

반응 단계

The title compound of Example 10 (12.0 g) was dissolved in 50 ml of dioxane to which was added 50 ml of 6M hydrogen chloride/dioxane. After about one hour, the volatiles were removed in vacuo and the residue triturated thoroughly with diethyl ether. The title compound (10.9 g) was collected as an analytically pure hydrochloride hemihydrate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04722922
출처 데이터셋uspto-grants-1988_02
ORD IDord-5cde0d6b47b04ae18f76dd684a697a17
출처 메모uspto-grants-1988_02