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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 715972생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/715972

반응식

참여 물질

역할이름HCID투입량
반응물Lithium ChlorideHCID 433294—
반응물Tert-butyl 2-tributylstannanylethynylpyrrolidine-1-carboxylateHCID 70984584—
반응물Methyl 2-(2,2-dimethylpropionylamino)-6-trifluoromethanesulfonyloxybenzoateHCID 86712118—
촉매HCID 178418476HCID 178418476—
용매DimethylformamideHCID 6228—
생성물Tert-butyl 2-[3-(2,2-dimethylpropionylamino)-2-methoxycarbonylphenylethynyl]-pyrrolidine-1-carboxylateHCID 7098293886.7%

반응 조건

온도95 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09187494B2
출처 데이터셋uspto-grants-2015_11
ORD IDord-a95fe76c005a4de5852ca2e20558e15c
출처 메모uspto-grants-2015_11