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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 504373생성일: 2026년 10월 26일

Tetrahydrofuran → (1R)-1'-{[1-(2-Fluoro-4-pyridin-4-ylphenyl)cyclopropyl]carbonyl}-3H-spiro[2-benzofuran-1,3'-pyrrolidin]-3-one

https://huagongshe.com/reaction/504373

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참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물tert-ButylphosphineHCID 123165—
반응물4-(Tri-n-butylstannyl)pyridineHCID 2737318—
반응물(1R)-1'-{[1-(4-bromo-2-fluorophenyl)cyclopropyl]carbonyl}-3H-spiro[2-benzofuran-1,3'-pyrrolidin]-3-oneHCID 66662680—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
생성물(1R)-1'-{[1-(2-Fluoro-4-pyridin-4-ylphenyl)cyclopropyl]carbonyl}-3H-spiro[2-benzofuran-1,3'-pyrrolidin]-3-oneHCID 66662043—

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온도120 °C

반응 단계

To a solution of (1R)-1′-{[1-(4-bromo-2-fluorophenyl)cyclopropyl]carbonyl}-3H-spiro[2-benzofuran-1,3′-pyrrolidin]-3-one (30 mg, 0.00007 mol, this compound was prepared by using a method that was analogous to that used for the synthesis of 238) in tetrahydrofuran (0.2 mL, 0.002 mol) were added tris(dibenzylideneacetone)dipalladium(0) (3 mg, 0.000003 mol), ti-tert-butylphosphine (1.7 mg, 0.0000083 mol), 4-(tributylstannyl)pyridine (30.7 mg, 0.0000835 mol), and the mixture was heated to 120° C. under microwave for 30 minutes. The reaction mixture was then filtered and the filtrate was diluted with methanol, and the product was isolated and purified by prep-HPLC. LC/MS (M+H+) 429.2.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07776874B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-00214c7bdbdc465db3a7a2ad7a18fd5e
출처 메모uspto-grants-2010_08