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Phenyl isocyanate → 2-Amino-4-(1-phenylcarbamoyl-4-piperidinyl)quinazoline
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Phenyl isocyanate | HCID 7672 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 2-Amino-4-(4-piperidinyl)quinazoline | HCID 15428775 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 2-Amino-4-(1-phenylcarbamoyl-4-piperidinyl)quinazoline | HCID 21851519 | 87% |
反応手順
To a solution of 2-amino-4-(4-piperidinyl)quinazoline (100 mg, 0.44 mmol) obtained in Example 11(1) and triethylamine (133 mg, 1.3 mmol) in dichloromethane (50 ml) was added phenyl isocyanate (50 mg, 0.42 mmol) under a nitrogen atmosphere. The mixture was stirred for about 3 hours at room temperature. The reaction mixture was washed with saturated sodium hydrogencarbonate aqueous solution. The organic layer was dried over sodium sulfate and evaporated in vacuo. The residue was purified by silicagel column chromatography (chloroform:methanol=99:1) to give the titled compound (127 mg).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05948786 |
| 出典データセット | uspto-grants-1999_09 |
| ORD ID | ord-91c7730f43df421a9a14133717031f4a |
| 出典メモ | uspto-grants-1999_09 |