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HRID 378282作成日:2026年10月25日

4,6-Dichloro-2-(pyrrolidin-1-yl)pyrimidine → N-[4-(6-chloro-2-pyrrolidin-1-yl-pyrimidin-4-ylsulfamoyl)-phenyl]-acetamide

https://huagongshe.com/reaction/378282

反応式

関与物質

役割名称HCID仕込み量
反応物4,6-Dichloro-2-(pyrrolidin-1-yl)pyrimidineHCID 19353553—
反応物N-(4-sulfamoyl-phenyl)-acetamide potassium saltHCID 70262342—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物N-[4-(6-chloro-2-pyrrolidin-1-yl-pyrimidin-4-ylsulfamoyl)-phenyl]-acetamideHCID 1064441466%

反応手順

0.58 g (0.00266 mol) of 4,6-dichloro-2-pyrrolidin-1-yl-pyrimidine and 1.36 g (0.00539 mol) of N-(4-sulfamoyl-phenyl)-acetamide potassium salt were stirred in 10 ml of 1-methyl-2-pyrrolidone at 140° C. for 8 hours. Then, the solvent was distilled off in a high vacuum, the residue was partitioned in ethyl acetate/water and extracted. The aqueous phase was made acid with 4N HCl and extracted with ethyl acetate. Both organic phases were combined and concentrated. The residue was recrystallized from a small amount of ethanol and the mother liquor was chromatographed over silica gel with cyclohexane/ethyl acetate 2:1 as the eluent. There was obtained a total of 0.62 g (66%) of N-[4-(6-chloro-2-pyrrolidin-1-yl-pyrimidin-4-ylsulfamoyl)-phenyl]-acetamide as whitish crystals; m.p. 229-233° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06030976
出典データセットuspto-grants-2000_02
ORD IDord-61b2fa2185554870b63b78aad13ef317
出典メモuspto-grants-2000_02