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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 647996생성일: 2026년 10월 26일

Phosphorus oxychloride → Isopropyl 3-p-fluorobenzoyl-5,6,7,8-tetrahydropyrrolo[1,2-a]pyridine-8-carboxylate

https://huagongshe.com/reaction/647996

반응식

참여 물질

역할이름HCID투입량
반응물Phosphorus oxychlorideHCID 24813—
반응물4-fluoro-N,N-dimethylbenzamideHCID 141077—
반응물Isopropyl 5,6,7,8-tetrahydropyrrolo[1,2-a]pyridine-8-carboxylateHCID 12795102—
반응물Sodium Acetate TrihydrateHCID 23665404—
용매1,2-DichloroethaneHCID 11—
용매WaterHCID 962—
생성물Isopropyl 3-p-fluorobenzoyl-5,6,7,8-tetrahydropyrrolo[1,2-a]pyridine-8-carboxylateHCID 20484013—

반응 단계

A solution of 758 mg. of N,N-dimethyl-4-fluorobenzamide and 0.44 ml. of phosphorous oxychloride in 50 ml. of 1,2-dichloroethane is refluxed for one hour. To this solution is added a solution of 500 mg. of isopropyl 5,6,7,8-tetrahydropyrrolo[1,2-a]pyridine-8-carboxylate in 10 ml. 1,2-dichloroethane. The reaction mixture is refluxed for 3 hours. A solution of 3.3 g. sodium acetate trihydrate in 9 ml water is added and refluxed for a further 10 hours. The organic phase is separated, washed with saturated sodium chloride solution, dried over sodium sulfate and evaporated to dryness. The residue is purified by preparative t.l.c. using hexane:ethyl acetate (90:10). Crystallization from dichloromethane-hexane yields isopropyl 3-p-fluorobenzoyl-5,6,7,8-tetrahydropyrrolo[1,2-a]pyridine-8-carboxylate (XI, R=H, L=p-F, R2 =iC3H7, n=1), m.p. 92° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04410534
출처 데이터셋uspto-grants-1983_10
ORD IDord-cc16e4974dda462b8218d8903d8cfca0
출처 메모uspto-grants-1983_10