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HRID 8896作成日:2026年10月25日

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

https://huagongshe.com/reaction/8896

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium BicarbonateHCID 516892—
反応物6-Methoxypyridine-3-carbaldehydeHCID 3364576—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物2-Amino-N-(4-bromo-3-trifluoromethylphenyl)benzamideHCID 11268358—
溶媒Acetic AcidHCID 176—
溶媒MethanolHCID 887—
生成物2-[[6-Methoxy-3-pyridinyl]methyl]amino-N-[4-bromo-3-(trifluoromethyl)phenyl]benzamideHCID 9913029—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07091224B2
出典データセットuspto-grants-2006_08
ORD IDord-30d829900b214d78b3ad1950f83d7458
出典メモuspto-grants-2006_08