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HRID 1830991생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1830991

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% EtOAc 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 번호US07067543B2
출처 데이터셋uspto-grants-2006_06
ORD IDord-11852088d3074b6fbabc22a433957904
출처 메모uspto-grants-2006_06