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2-(Benzenesulfonyl)-3-phenyloxaziridine → 2-Amino-4-methanesulfinyl-6-phenoxy-pyrimidine-5-carbonitrile
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-(Benzenesulfonyl)-3-phenyloxaziridine | HCID 320405 | — |
| 反応物 | 2-Amino-4-methylsulfanyl-6-phenoxy-pyrimidine-5-carbonitrile | HCID 18507391 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 2-Amino-4-methanesulfinyl-6-phenoxy-pyrimidine-5-carbonitrile | HCID 18507344 | 27% |
反応手順
To a stirred suspension of 950 mg (3.68 mmol) 2-amino-4-methylsulfanyl-6-phenoxy-pyrimidine-5-carbonitrile in 20 ml dichloromethane was added 3.84 g (14.7 mmol) 3-phenyl-2-(phenylsulfonyl)oxaziridine and stirring continued for 24 hours at room temperature. The reaction mixture was then concentrated in vacuo and the residue resuspended in ether/hexane and filtered to afford 270 mg (27%) 2-amino-4-methanesulfinyl-6-phenoxy-pyrimidine-5-carbonitrile as a light yellow crystalline solid. ES-MS m/e (%): 275 (M+H+, 100).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06586441B2 |
| 出典データセット | uspto-grants-2003_07 |
| ORD ID | ord-33282ad0247142cab6529b07968f00c5 |
| 出典メモ | uspto-grants-2003_07 |