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HRID 1623795作成日:2026年10月26日

1,2-Dichloroethane → HCID 67108081、化合物

https://huagongshe.com/reaction/1623795

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-DichloroethaneHCID 11—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物2-Fluoropyridin-3-amineHCID 2762816—
反応物2-(Benzyloxy)-5-(pyridin-4-yl)benzoic acidHCID 66990482—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物HCID 67108081HCID 67108081—

反応条件

温度25 °C

反応手順

A solution of 2-[(phenylmethyl)oxy]-5-(4-pyridinyl)benzoic acid (may be prepared as described in Description 79; 0.12 g, 0.34 mmol), EDC (0.16 g, 0.84 mmol) and HOBT (0.13 g, 0.84 mmol) in dimethylformamide (2 ml) was stirred in air at room temperature for 1 h. 2-Fluoropyridin-3-amine (0.04 g, 0.37 mmol) was then added in one charge. The reaction mixture was stirred at 25° C. overnight. Another batch of HOBT (0.13 g, 0.84 mmol), EDC (0.161 g, 0.842 mmol) and 2-fluoropyridin-3-amine (0.04 g, 0.37 mmol) was added into the mixture and heating was continued at 40° C. for 38 hours. The reaction mixture was diluted with water (30 ml) and extracted with ethyl acetate (60 ml×3). The organic phases were combined, washed with brine (50 ml×3), dried over anhydrous MgSO4, and concentrated. The residue was purified by chromatography (silica gel, 40 g, eluent: dichloromethane/methanol=50:1, 1 L). The solid was washed by methanol (3 ml×2) and dried in vacuo to yield the title compound as a grey solid. 31 mg.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08778939B2
出典データセットuspto-grants-2014_07
ORD IDord-1432107721e24f09a13cf0c66b754ca1
出典メモuspto-grants-2014_07