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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2180118생성일: 2026년 10월 26일

Triphenylphosphine → 4-Chloro-6-methoxy-7-(3-(pyrrolidin-1-yl)propoxy)cinnoline

https://huagongshe.com/reaction/2180118

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물1-PyrrolidinepropanolHCID 209342—
반응물ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
반응물4-Chloro-7-hydroxy-6-methoxycinnolineHCID 135752523—
용매DichloromethaneHCID 6344—
생성물4-Chloro-6-methoxy-7-(3-(pyrrolidin-1-yl)propoxy)cinnolineHCID 1127869018%

반응 단계

To a solution of 4-chloro-7-hydroxy-6-methoxycinnoline (300 mg, 1.42 mmol), triphenylphosphine (747 mg, 2.85 mmol) and 3-(pyrrolidin-1-yl)propan-1-ol (276 mg, 2.1 mmol) in methylene chloride (12 ml) was added diethyl azodicarboxylate (449 μl, 2.85 mmol) dropwise and the mixture was stirred for 2 hours at ambient temperature. The volatiles were removed under vacuum and the residue was purified by column chromatography eluting with methylene chloride/methanol (90/10) followed by methylene chloride/methanol/methanol saturated with ammonia (89/10/1 followed by 85/10/5). The fractions containing the expected product were combined and evaporated to give 4-chloro-6-methoxy-7-(3-(pyrrolidin-1-yl)propoxy)cinnoline (80 mg, 18%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06887874B2
출처 데이터셋uspto-grants-2005_05
ORD IDord-69bbf242a4eb4472863103edf67ac4cc
출처 메모uspto-grants-2005_05