돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1882923생성일: 2026년 10월 27일

Sodium borohydride → N-(6-chloropyridin-3-yl)-2-aminobenzamide

https://huagongshe.com/reaction/1882923

반응식

참여 물질

역할이름HCID투입량
반응물Sodium borohydrideHCID 4311764—
반응물N-(6-chloropyridin-3-yl)-2-nitrobenzamideHCID 21906170—
촉매Nickel acetate tetrahydrateHCID 62601—
용매MethanolHCID 887—
용매TetrahydrofuranHCID 8028—
생성물N-(6-chloropyridin-3-yl)-2-aminobenzamideHCID 2190654946%

반응 단계

To a stirred solution of N-(6-chloropyridin-3-yl)-2-nitrobenzamide (0.6 g, 2.15 mmol) in methanol (150 mL) and tetrahydrofuran (75 mL) was added nickel acetate tetrahydrate (1.07 g, 4.3 mmol). Sodium borohydride (0.326 g, 8.61 mmol) was then added in small portions. After gas evolution had ceased, the solvent was removed in vacuo. The residue was partitioned between ethyl acetate and concentrated ammonium hydroxide, and the layers separated. The organic phase was washed with concentrated ammonium hydroxide and saturated aqueous sodium chloride solution, dried (magnesium sulfate), filtered, and concentrated in vacuo. The solid was suspended in ether, sonicated, and filtered to give 0.243 g (46%) of a pink solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06759414B2
출처 데이터셋uspto-grants-2004_07
ORD IDord-0d27dd0e9a2148d9841a3d4206b39f26
출처 메모uspto-grants-2004_07