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HRID 43394作成日:2026年10月24日

1,2-Dichloroethane → (2S)-1-[(4-Chlorophenyl)sulfonyl]-2-methyl-4-[(6-methyl-3-pyridinyl)carbonyl]piperazine

https://huagongshe.com/ja/reaction/43394

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EthylmorpholineHCID 7525—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物6-Methylnicotinic acidHCID 137860—
反応物(2S)-1-[(4-Chlorophenyl)sulfonyl]-2-methylpiperazine hydrochlorideHCID 67028562—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物(2S)-1-[(4-Chlorophenyl)sulfonyl]-2-methyl-4-[(6-methyl-3-pyridinyl)carbonyl]piperazineHCID 5916139841.3%

反応手順

To a suspension of (2S)-1-[(4-chlorophenyl)sulfonyl]-2-methylpiperazine hydrochloride (Description 4) (105 mg, 0.338 mmol), EDC (71.2 mg, 0.371 mmol), HOBT.H2O (56.9 mg, 0.371 mmol) and 6-methyl-3-pyridinecarboxylic acid (51.0 mg, 0.372 mmol) in DCM (5 ml) was added N-ethylmorpholine (0.090 ml, 0.710 mmol). The reaction was stirred for 18 h at ambient temperature. To the reaction was added water (3 ml) and the organic layer collected via a hydrophobic frit. The organic layer was reduced in volume to approximately 2 ml then loaded onto a silica SP4 chromatography cartridge. The cartridge was eluted with ethyl acetate then a gradient from 0-10% (20% methanol in dichloromethane) in ethyl. Fractions containing the desired product were combined and reduced in vacuo to yield the title compound as a white solid (55 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08536183B2
出典データセットuspto-grants-2013_09
ORD IDord-5ea037a08ea043bf8ede033f0ff8dad6
出典メモuspto-grants-2013_09