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HRID 715972作成日:2026年10月25日

Lithium Chloride → Tert-butyl 2-[3-(2,2-dimethylpropionylamino)-2-methoxycarbonylphenylethynyl]-pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/715972

反応式

関与物質

役割名称HCID仕込み量
反応物Lithium ChlorideHCID 433294—
反応物Tert-butyl 2-tributylstannanylethynylpyrrolidine-1-carboxylateHCID 70984584—
反応物Methyl 2-(2,2-dimethylpropionylamino)-6-trifluoromethanesulfonyloxybenzoateHCID 86712118—
触媒HCID 178418476HCID 178418476—
溶媒DimethylformamideHCID 6228—
生成物Tert-butyl 2-[3-(2,2-dimethylpropionylamino)-2-methoxycarbonylphenylethynyl]-pyrrolidine-1-carboxylateHCID 7098293886.7%

反応条件

温度95 °C

反応手順

A mixture of methyl 2-(2,2-dimethylpropionylamino)-6-trifluoromethanesulfonyloxybenzoate (Intermediate 39, 3.83 g), tert-butyl 2-tributylstannanylethynyl-pyrrolidine-1-carboxylate (Intermediate 41, 5.81 g), bis(triphenylphosphine)palladium(II) dichloride (0.702 g) and lithium chloride (1.28 g) in dimethylformamide (50 mL) was stirred and heated at 95° C. under nitrogen for 1 hour. After cooling, the mixture was concentrated in vacuo and the residue was partitioned between ethyl acetate and water. The organic layer was washed with water, dried (Na2SO4) and filtered. The filtrate was concentrated in vacuo and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane with a gradient of 0-25% to give tert-butyl 2-[3-(2,2-dimethylpropionylamino)-2-methoxycarbonyl-phenylethynyl]-pyrrolidine-1-carboxylate (3.71 g) as a viscous gum.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09187494B2
出典データセットuspto-grants-2015_11
ORD IDord-a95fe76c005a4de5852ca2e20558e15c
出典メモuspto-grants-2015_11