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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1044646생성일: 2026년 10월 26일

4-Methylmorpholine → Boc-Ala-Ala-NH-(CH2)4-OH

https://huagongshe.com/reaction/1044646

반응식

참여 물질

역할이름HCID투입량
반응물4-MethylmorpholineHCID 7972—
반응물Ethyl chloroformateHCID 10928—
반응물4-Amino-1-butanolHCID 25868—
반응물N-((1,1-Dimethylethoxy)carbonyl)-L-alanyl-L-alanineHCID 6992569—
용매TetrahydrofuranHCID 8028—
생성물Boc-Ala-Ala-NH-(CH2)4-OHHCID 5953708075%

반응 단계

To a vigorously stirring solution of Boc-(Ala)2-OH (0.9 gm, 3.46 mmol) and NMM (0.57 mL, 5.2 mmol) in THF (20 mL) cooled to −15° C. was added under N2 atmosphere ethyl chloroformate (ECF) (372 μL, 3.56 mmol) and stirred for 2 min. A solution of H2N(CH2)4OH (462 mg, 5.19 mmol) in THF (5 mL) was added to the mixture followed by NMM (950 μL, 8.65 mmol) and the mixture was warmed to r.t. and stirred until silica gel TLC indicated complete consumption of the starting acid (eluting solvent—MeOH:DCM—1:10, Rf—0.45) (˜8 h). The solvent was evaporated, and the residue was diluted with EtOAc and washed with brine, water, saturated solutions of citric acid and NaHCO3, and the organic layer was dried using NaHSO4, and the solvent was removed under vacuum to yield a residue which was purified using silica gel flash column chromatography—Hexanes:EtOAc—1:3; to give the desired product in 75% yield (858 mg) as a solid—m.p.—102-104° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08563686B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-bd9d8cd11099458aa2f8c3dce2987f7f
출처 메모uspto-grants-2013_10