化工社化工社 化学情報印刷レポート · 研究参考用
Benzene, 1-chloro-3-isocyanato- → 1(m-nitrophenyl)-3-allylquinazoline-2,4(1H, 3H)-dione
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Benzene, 1-chloro-3-isocyanato- | HCID 17968 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | 2-(m-nitroanilino)-N-allylbenzamide | HCID 21444004 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 1(m-nitrophenyl)-3-allylquinazoline-2,4(1H, 3H)-dione | HCID 13272344 | 70.5% |
反応手順
3.0 g of 2-(m-nitroanilino)-N-allylbenzamide was dissolved in 20 ml of tetrahydrofuran. To the solution was added 1.0 g of approximately 50 % sodium hydride and stirring was performed for 30 minutes. To this was added dropwise under cooling 4.6 g of m-chlorophenyl isocyanate, and the mixture was stirred for one hour, and then refluxed for 5 hours. After the reaction was complete, the solvent was distilled off from the resulting mixture. The residue thus obtained was recrystallized from methanol to give 2.3 g of 1-(m-nitrophenyl)-3-allylquinazoline-2,4(1H, 3H)-dione as colorless needles, melting at 165°-166° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04016166 |
| 出典データセット | uspto-grants-1977_04 |
| ORD ID | ord-519dbbb3c2ea4057b55b69026901ce1e |
| 出典メモ | uspto-grants-1977_04 |