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HRID 1012161作成日:2026年10月27日

1,2-Dichloroethane → HCID 178522446、化合物

https://huagongshe.com/reaction/1012161

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TriethylamineHCID 8471—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物6-Chloropyridine-3,4-diamineHCID 817133—
反応物HCID 178524951HCID 178524951—
溶媒DimethylformamideHCID 6228—
生成物HCID 178522446HCID 1785224466.5%

反応手順

A mixture of 4-(2,6-difluorobenzylamino)-1H-pyrazole-3-carboxylic acid (100 mg, 0.37 mmol) (Example 16D), 6-chloro-pyridine-3,4-diamine (54 mg, 0.37 mmol), EDC (72 mg, 0.40 mmol), HOBt (57.3 mg, 0.40 mmol) and Et3N (0.075 ml, 0.55 mmol) in DMF (20 ml) was stirred at ambient temperature for 48 h and then partitioned between EtOAc and saturated aqueous sodium bicarbonate and the organic portion dried (MgSO4), filtered and evaporated. The amide intermediate was dissolved in AcOH (3 ml), heated at reflux for 1 h, and then heated in the microwave (150 W) at 160° C. until the reaction was complete. The reaction mixture was allowed to cool, a solid crystallised out, which was filtered and then washed with petroleum ether and dried to give the required product (9 mg). (LC/MS: Rt 2.74, [M+H]+ 375)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07977477B2
出典データセットuspto-grants-2011_07
ORD IDord-3cd9bfea20264e5cb6f277b84ad2b8a7
出典メモuspto-grants-2011_07