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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1471849생성일: 2026년 10월 24일

Triethylamine → 1-(2,2-difluorobenzo-[d][1,3]dioxol-5-yl)-N-(1-(6-oxo-1,6-dihydropyridin-3-yl)isoquinolin-3-yl)cyclopropane-carboxamide

https://huagongshe.com/ko/reaction/1471849

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물1-(2,2-Difluorobenzo[d][1,3]dioxol-5-yl)-N-(1-(6-methoxypyridin-3-yl)isoquinolin-3-yl)cyclopropanecarboxamideHCID 57733010—
용매Hydrochloric AcidHCID 313—
용매1,4-DioxaneHCID 31275—
생성물1-(2,2-difluorobenzo-[d][1,3]dioxol-5-yl)-N-(1-(6-oxo-1,6-dihydropyridin-3-yl)isoquinolin-3-yl)cyclopropane-carboxamideHCID 57733024—

반응 조건

온도90 °C

반응 단계

1-(2,2-Difluorobenzo[d][1,3]dioxol-5-yl)-N-(1-(6-methoxypyridin-3-yl)isoquinolin-3-yl)cyclopropanecarboxamide (100 mg, 0.210 mmol) was dissolved in a mixture of 1.2 mL of 1,4-dioxane and 0.6 mL of 4M aqueous hydrochloric acid. The solution was heated at 90° C. for 2 hours. The crude reaction mixture was quenched with one equivalent of triethylamine and was then evaporated to dryness. The crude product was partitioned between dichloromethane and water. The organic layer was separated, dried over sodium sulfate, and a portion of the material was purified on 12 g of silica gel utilizing a gradient of 0-10% methanol in dichloromethane to yield 1-(2,2-difluorobenzo-[d][1,3]dioxol-5-yl)-N-(1-(6-oxo-1,6-dihydropyridin-3-yl)isoquinolin-3-yl)cyclopropane-carboxamide as a white solid. ESI-MS m/z calc. 461.1. found 461.9 (M+1)+. Retention time 1.67 minutes.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09012473B2
출처 데이터셋uspto-grants-2015_04
ORD IDord-20b92abfb0c04ae982998a37ad4cd938
출처 메모uspto-grants-2015_04