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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 12164생성일: 2026년 10월 25일

Sodium borohydride → [4-(Aminomethyl)phenyl]-n-{2-[n-(5-chloro(2-pyridyl))carbamoyl]phenyl}carboxamide

https://huagongshe.com/reaction/12164

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참여 물질

역할이름HCID투입량
반응물Sodium borohydrideHCID 4311764—
반응물n-{2-[n-(5-Chloro(2-pyridyl))carbamoyl]phenyl}(4-cyanophenyl)carboxamideHCID 22596336—
촉매Cobalt(II) chlorideHCID 24288—
용매DimethylformamideHCID 6228—
생성물[4-(Aminomethyl)phenyl]-n-{2-[n-(5-chloro(2-pyridyl))carbamoyl]phenyl}carboxamideHCID 1872760832.3%

반응 단계

A mixture of N-{2-[N-(5-chloro(2-pyridyl))carbamoyl]phenyl}(4-cyanophenyl)carboxamide (1 g, 2.6 mmol, 1.0 equiv.), cobalt chloride (0.5 g, 3.85 mmol, 1.5 equiv.) and sodium borohydride (0.295 g, 7.8 mmol, 3.0 equiv.) in DMF (20 mL) was stirred at 0° C. to rt for 2.5 hr. The reaction was quenched with ice cubes, diluted with ethyl acetate (100 mL) and filtered through celite. The filtrate was washed with saturated aqueous NaHCO3. The organic layer was dried over MgSO4, filtered, evaporated and HPLC (C18 reversed phase) eluting with 0.1% TFA in H2O/CH3CN gave [4-(aminomethyl)phenyl]-N-{2-[N-(5-chloro(2-pyridyl))carbamoyl]phenyl}carboxamide (320 mg, 30%). MS found for C20H17ClN4O2 (M+H)+: 381.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07727981B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-a33abca967ae4d04826e526108b5ff3e
출처 메모uspto-grants-2010_06