돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1024194생성일: 2026년 10월 24일

Sodium hydride → (1H-pyrrolo[2,3-b]pyridin-3-yl)-[6-(3-trifluoromethyl-benzyloxy)-pyridin-3-yl]-methanone

https://huagongshe.com/ko/reaction/1024194

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물3-(Trifluoromethyl)benzylic alcoholHCID 67681—
반응물(6-Chloro-pyridin-3-yl)-(1H-pyrrolo[2,3-b]pyridin-3-yl)-methanoneHCID 57588066—
용매Dimethyl SulfoxideHCID 679—
생성물(1H-pyrrolo[2,3-b]pyridin-3-yl)-[6-(3-trifluoromethyl-benzyloxy)-pyridin-3-yl]-methanoneHCID 59593361—

반응 조건

온도60 °C

반응 단계

To (6-Chloro-pyridin-3-yl)-(1H-pyrrolo[2,3-b]pyridin-3-yl)-methanone 7 in DMSO was added (3-trifluoromethyl-phenyl)-methanol 72. Sodium hydride was added and the reaction was heated to 60° C. for two hours. The reaction was quenched with water and extracted with ethyl acetate. The organic portion was dried with magnesium sulfate and concentrated to provide (1H-pyrrolo[2,3-b]pyridin-3-yl)-[6-(3-trifluoromethyl-benzyloxy)-pyridin-3-yl]-methanone 73, which was used in the next step without additional purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08722702B2
출처 데이터셋uspto-grants-2014_05
ORD IDord-7593811251104b8d83f77363e00b04e7
출처 메모uspto-grants-2014_05