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HRID 1584193作成日:2026年10月26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/1584193
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | 4,6-Dichloro-2-(pyrrolidin-1-yl)pyrimidine | HCID 19353553 | — |
| 反応物 | N-(4-sulfamoyl-phenyl)-acetamide potassium salt | HCID 70262342 | — |
| 溶媒 | N-methyl-2-pyrrolidone | HCID 13387 | — |
| 生成物 | N-[4-(6-chloro-2-pyrrolidin-1-yl-pyrimidin-4-ylsulfamoyl)-phenyl]-acetamide | HCID 10644414 | 66% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05932599 |
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| 出典データセット | uspto-grants-1999_08 |
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| ORD ID | ord-74d0163a864c406b98791ae706bc7313 |
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| 出典メモ | uspto-grants-1999_08 |
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