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HRID 1635114생성일: 2026년 10월 27일

Ammonia → Butanedioic acid, 1,4-di-2-propen-1-yl ester

https://huagongshe.com/reaction/1635114

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물DiisopropylethylamineHCID 81531—
반응물SuccinateHCID 160419—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
용매DimethylformamideHCID 6228—
생성물Butanedioic acid, 1,4-di-2-propen-1-yl esterHCID 70215—

반응 단계

11 (240 mg, 0.46 mmol) and HATU (350 mg, 0.92 mmol) were dissolved in DMF (2 mL) and diisopropylethylamine (0.16 mL, 0.92 mmol) was added. The mixture was stirred for 15 min at ambient temperature, and then treated with anhydrous ammonia for 20 min. Stirring was continued overnight. DMF was removed in vacuo, and the residue was diluted with ethyl acetate, washed with water and brine, then dried over MgSO4. After evaporation of the solvent, the residue was purified on silica gel (5% methanol/methylene chloride) to afford product 12 as a white solid. 12, a mixture of two diastereomers, was then separated on silica gel, using increasing gradient of 20-50% ethyl acetate-methylene chloride, to give first eluting isomer 12a (43 mg, 18%) and the second eluting isomer 12b (61 mg, 25%) both as a white solids. 12a: MS m/z 521.2 (MH+). 12b: MS m/z 521.2 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06509333B2
출처 데이터셋uspto-grants-2003_01
ORD IDord-2e9162714d7b4ab5a5d53fa9d1dec73b
출처 메모uspto-grants-2003_01