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HRID 2227260作成日:2026年10月26日

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

https://huagongshe.com/reaction/2227260

反応式

関与物質

役割名称HCID仕込み量
反応物tert-Butyl DimethylphosphonoacetateHCID 4564495—
反応物[4-(6-Methoxy-pyridin-3-yl)-4-oxo-butyl]-carbamic Acid tert-Butyl EsterHCID 22086439—
反応物Sodiumbis(trimethylsilylamide)HCID 86599718—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物6-tert-Butoxycarbonylamino-3-(6-methoxy-pyridin-3-yl)-hex-2-enoic Acid tert-Butyl EsterHCID 69987906—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06413955B1
出典データセットuspto-grants-2002_07
ORD IDord-37ac060b518c4f7a8b14c5df320cc9c6
出典メモuspto-grants-2002_07