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HRID 2227260생성일: 2026년 10월 26일

tert-Butyl Dimethylphosphonoacetate → 6-tert-Butoxycarbonylamino-3-(6-methoxy-pyridin-3-yl)-hex-2-enoic Acid tert-Butyl Ester

https://huagongshe.com/reaction/2227260

반응식

참여 물질

역할이름HCID투입량
반응물tert-Butyl DimethylphosphonoacetateHCID 4564495—
반응물[4-(6-Methoxy-pyridin-3-yl)-4-oxo-butyl]-carbamic Acid tert-Butyl EsterHCID 22086439—
반응물Sodiumbis(trimethylsilylamide)HCID 86599718—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물6-tert-Butoxycarbonylamino-3-(6-methoxy-pyridin-3-yl)-hex-2-enoic Acid tert-Butyl EsterHCID 69987906—

반응 단계

To a stirred solution of t-butyl dimethylphosphonoacetate (6.86 g, 30.6 mmol) in tetrahydrofuran (150 mL) at −78° C. under argon was added a solution of sodium bis(trimethylsilylamide) (30.6 mL of a 1.0 M solution). After 15 min., a solution of 1-3 (3.0 g, 10.2 mmol) in tetrahydrofuran (30 mL) was added, and the reaction was warmed to ambient temperature, then heated to 40° C. for 1 h. The reaction mixture was then cooled to ambient temperature, diluted with ethyl acetate and washed with saturated aqueous sodium hydrogen carbonate, then saturated aqueous sodium chloride, and dried over anhydrous magnesium sulfate. The reaction mixture was filtered and concentrated at reduced pressure to give an oil that was purified by flash column chromatography (silica gel, 15 to 25% ethyl acetate/hexanes) to give 1-4 and its 2 isomer.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06413955B1
출처 데이터셋uspto-grants-2002_07
ORD IDord-37ac060b518c4f7a8b14c5df320cc9c6
출처 메모uspto-grants-2002_07