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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 8896생성일: 2026년 10월 23일

Sodium Bicarbonate → 2-[[6-Methoxy-3-pyridinyl]methyl]amino-N-[4-bromo-3-(trifluoromethyl)phenyl]benzamide

https://huagongshe.com/ko/reaction/8896

반응식

참여 물질

역할이름HCID투입량
반응물Sodium BicarbonateHCID 516892—
반응물6-Methoxypyridine-3-carbaldehydeHCID 3364576—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물2-Amino-N-(4-bromo-3-trifluoromethylphenyl)benzamideHCID 11268358—
용매Acetic AcidHCID 176—
용매MethanolHCID 887—
생성물2-[[6-Methoxy-3-pyridinyl]methyl]amino-N-[4-bromo-3-(trifluoromethyl)phenyl]benzamideHCID 9913029—

반응 단계

Sodium cyanoborohydride (8.80 g of 95%, 133 mmol) is added in portions over 30 minutes to a stirred mixture of acetic acid (3.8 mL), 6-methoxy-3-pyridinecarboxaldehyde (Fluka, Buchs, Switzerland; 7.80 g, 57 mmol) and 2-amino-N-(4-bromo-3-trifluoromethylphenyl)-benzamide (step 1.2; 13.65 g, 38 mmol) in methanol (380 mL) at 25° C. The mixture is stirred for 16 hours. The solvent is evaporated under reduced pressure to give a residue which is treated with a saturated aqueous solution of sodium hydrogen carbonate (500 mL) and extracted with dichloromethane (3×150 mL). The combined extracts are dried (Na2SO4), filtered and the solvent is evaporated under reduced pressure to yield the crude product that is purified by column chromatography on silica gel, eluent 5% ethyl acetate in dichloromethane and recrystallised from diethylether-hexane to give the title compound as a beige crystalline solid, m.p. 101–103° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091224B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-30d829900b214d78b3ad1950f83d7458
출처 메모uspto-grants-2006_08