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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 27347생성일: 2026년 10월 25일

4-Methylmorpholine → carbobenzoxy-beta-alanyl-L-proline t-butyl ester

https://huagongshe.com/reaction/27347

반응식

참여 물질

역할이름HCID투입량
반응물4-MethylmorpholineHCID 7972—
반응물Isobutyl chloroformateHCID 62365—
반응물N-Benzyloxycarbonyl-beta-alanineHCID 75313—
반응물tert-Butyl L-prolinate hydrochlorideHCID 6453107—
용매DimethylformamideHCID 6228—
용매TetrahydrofuranHCID 8028—
용매TriethylamineHCID 8471—
생성물carbobenzoxy-beta-alanyl-L-proline t-butyl esterHCID 54135485—

반응 단계

4.46 g. of carbobenzoxy-β-alanine is dissolved in 20 ml. of tetrahydrofuran and the resulting solution cooled to -10° C. With constant stirring of the solution, 2.4 ml. of N-methylmorpholine followed by 2.6 ml. of isobutylchloroformate are added and the resulting reaction mixture is stirred thereafter for approximately 5 minutes at -10° C. 4.16 g. of L-proline t-butyl ester hydrochloride in 20 ml. of dimethylformamide and 2.8 ml. of triethylamine is added to the reaction mixture which is thereafter stirred overnight, while slowly warming to room temperature. The solvent of the reaction mixture is evaporated in vacuo at 30°-35°. The residue is dissolved in 800 ml. of ethyl acetate which is washed with (2×150 ml.) a 10% citric acid solution, with (1×150 ml.) water, with (2×150 ml.) saturated solution of sodium bicarbonate and then with (2×100 ml.) water. The organic layer is dried with anhydrous magnesium sulfate and the solvent evaporated to yield carbobenzoxy-β-alanyl-L-proline t-butyl ester.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04221706
출처 데이터셋uspto-grants-1980_09
ORD IDord-c7cd6af73aca49feafad7a587907044d
출처 메모uspto-grants-1980_09