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HRID 1242839作成日:2026年10月24日

Dimethylacetoacetamide → tert-Butyl 2-(3-Methoxycarbonyladamant-1-ylcarbonylamino)-6-(N,N-dimethylaminocarbonyl)hex-4-ynoate

https://huagongshe.com/ja/reaction/1242839

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylacetoacetamideHCID 16278—
反応物tert-Butyl 2-(3-methoxycarbonyladamant-1-ylcarbonylamino)pent-4-ynoateHCID 21940505—
触媒Copper SulfateHCID 24462—
溶媒BenzeneHCID 241—
生成物tert-Butyl 2-(3-Methoxycarbonyladamant-1-ylcarbonylamino)-6-(N,N-dimethylaminocarbonyl)hex-4-ynoateHCID 21940554—

反応手順

tert-Butyl 2-(3-methoxycarbonyladamant-1-ylcarbonylamino)pent-4-ynoate (0.44 g) was dissolved in 0.8 mL of dry benzene under nitrogen. To this solution was added a catalytic amount of CuSO4 and the reaction mixture was brought to reflux. N,N-Dimethyl acetoacetamide was added dropwise in excess. Evolution of nitrogen was observed. The addition was complete after 30 min. The reaction was then heated for another 30 min. After cooling the reaction mixture, the solvent was evaporated under reduced pressure and the crude product was purified on a prep plate (silica gel; EtOAc/hexanes, 2:3) to afford the title compound as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07115768B2
出典データセットuspto-grants-2006_10
ORD IDord-9ee51b8828e64373a76bf75068b9ca6f
出典メモuspto-grants-2006_10