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HRID 8900作成日:2026年10月24日

Sodium Hydroxide → [6-Methoxy-3-pyridinyl]methylamino-N-[4-(1-propynyl)-3-(trifluoromethyl)phenyl]benzamide

https://huagongshe.com/ja/reaction/8900

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物Tributyl(prop-1-yn-1-yl)stannaneHCID 2733165—
反応物2-[[6-Methoxy-3-pyridinyl]methyl]amino-N-[4-bromo-3-(trifluoromethyl)phenyl]benzamideHCID 9913029—
触媒HCID 178418397HCID 178418397—
溶媒TolueneHCID 1140—
生成物[6-Methoxy-3-pyridinyl]methylamino-N-[4-(1-propynyl)-3-(trifluoromethyl)phenyl]benzamideHCID 9980607—

反応条件

温度100 °C

反応手順

A stirred solution of 2-[[6-methoxy-3-pyridinyl]methyl]amino-N-[4-bromo-3-(trifluoromethyl)-phenyl]benzamide (Reference Example 1; 3.98 g, 8.3 mmol) in dry toluene (200 mL) is purged with argon for 20 minutes at 25° C. Tributyl-1-propynylstannane (4.1 g of 80%, 9.96 mmol) and tetrakis(triphenylphosphine)palladium (0) (260 mg) are then added and the resulting mixture is heated at 100° C. for 17 hours under an argon atmosphere. The mixture is then cooled, treated with an aqueous solution of sodium hydroxide (85 mL of 0.1 M) and purged with air for 2 hours. The resulting mixture is extracted with ethyl acetate (3×100 mL). The organic phase is sequentially washed with water (2×40 mL) and saturated aqueous sodium chloride (1×40 mL), dried (Na2SO4), filtered and the solvent is evaporated under reduced pressure to yield the crude product which is purified by column chromatography on silica gel, eluent 33% ethyl acetate in hexane and recrystallised from diethylether-hexane to give the title compound as a pale-yellow crystalline solid; m.p. 123–124° 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-eb3583fec4e14b0cba6036c1e267daa2
出典メモuspto-grants-2006_08