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Hydrochloric Acid → 5-Bromo-n4-isopropyl-n2-(4-methylsulphanylphenyl)pyrimidine-2,4-diamine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | chloramine-T trihydrate | HCID 517414 | — |
| 反応物 | 5-Bromo-n4-isopropyl-n2-(4-methyl-sulphanylphenyl)pyrimidine-2,4-diamine | HCID 131728842 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | 5-Bromo-n4-isopropyl-n2-(4-methylsulphanylphenyl)pyrimidine-2,4-diamine | HCID 59674070 | — |
反応手順
1.36 g (4.8 mmol) of chloramine-T trihydrate (Aldrich) are added to a suspension of 1.56 g (4.0 mmol) of the hydrochloride of 5-bromo-N4-isopropyl-N2-(4-methyl-sulphanylphenyl)pyrimidine-2,4-diamine in 20 ml of acetonitrile at room temperature. The mixture is stirred at room temperature for 16 hours and then diluted with ethyl acetate. The mixture is filtered with suction and the filter cake is washed with ethyl acetate. The combined organic phases are dried (Na2SO4), filtered and concentrated. The resulting residue is purified by HPLC:
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07943629B2 |
| 出典データセット | uspto-grants-2011_05 |
| ORD ID | ord-038419359e4a4eff90deb757ec39e87f |
| 出典メモ | uspto-grants-2011_05 |