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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 922851생성일: 2026년 10월 27일

Acetic Acid → N-(4-chloro-3-(pyridin-2-yl)phenyl)-4-((dimethylamino)methyl)benzamide

https://huagongshe.com/reaction/922851

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물FormaldehydeHCID 712—
반응물DimethylformamideHCID 6228—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물4-(aminomethyl)-N-(4-chloro-3-(pyridin-2-yl)phenyl)benzamideHCID 66877992—
생성물N-(4-chloro-3-(pyridin-2-yl)phenyl)-4-((dimethylamino)methyl)benzamideHCID 58614907—

반응 단계

Procedure G was used to couple BOC-4-(aminomethyl)benzoic acid (48 mg) with 4-chloro-3-(pyridin-2-yl)aniline (35 mg). The crude reaction mixture was treated with TFA (1 mL) containing trace amounts of water for 1 h. The reaction mixture was concentrated to yield 4-(aminomethyl)-N-(4-chloro-3-(pyridin-2-yl)phenyl)benzamide. 4-(aminomethyl)-N-(4-chloro-3-(pyridin-2-yl)phenyl)benzamide (80 mg) was dissolved in DMF (5 mL) and treated with AcOH (10 L), paraformaldehyde (48 mg), and sodium triacetoxyborohydride (125 mg) for 16 h. The reaction mixture was concentrated, and the crude residue was dissolved in ethyl acetate and washed with 1 N sodium hydroxide, dried (MgSO4) and concentrated. The crude product was purified by reverse phase HPLC to yield N-(4-chloro-3-(pyridin-2-yl)phenyl)-4-((dimethylamino)methyl)benzamide. MS (Q1) 365.0 (M)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09278961B2
출처 데이터셋uspto-grants-2016_03
ORD IDord-a98e85eabba64752bf14d90ebc9bb51e
출처 메모uspto-grants-2016_03