돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1913671생성일: 2026년 10월 25일

Dimethylformamide → 2-(3-Cyclopentyloxypyridin-4-yl)-5-(trifluoromethyl)benzoxazole

https://huagongshe.com/reaction/1913671

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물BromocyclopentaneHCID 8728—
반응물Potassium CarbonateHCID 11430—
반응물4-[5-(Trifluoromethyl)benzoxazole-2-yl]pyridin-3-olHCID 136331268—
용매WaterHCID 962—
생성물2-(3-Cyclopentyloxypyridin-4-yl)-5-(trifluoromethyl)benzoxazoleHCID 6688022083.3%

반응 조건

온도60 °C

반응 단계

To a mixture of 0.28 g of 4-[5-(trifluoromethyl)benzoxazole-2-yl]pyridin-3-ol, 0.28 g of potassium carbonate and 2 ml of DMF, a mixture of 0.29 g of cyclopentyl bromide and 2 ml of DMF was added at room temperature. The reaction mixture was stirred while heating at 60° C. for four hours. The reaction mixture was cooled to room temperature, and then water was added to the reaction mixture, followed by extraction with ethyl acetate twice. The combined organic layers were washed with water and a saturated sodium chloride solution, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to give 0.29 g of 2-(3-cyclopentyloxypyridin-4-yl)-5-(trifluoromethyl)benzoxazole (hereinafter, referred to as “active compound 115”).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08609705B2
출처 데이터셋uspto-grants-2013_12
ORD IDord-6ba03f1821ac4b9aa8bc2a75d6dac585
출처 메모uspto-grants-2013_12