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HRID 1533129作成日:2026年10月25日
Di-tert-butyl dicarbonate → 4-(6,7-Dimethoxy-4-quinazolinyl)-N-(3-isopropylphenyl)-1-piperazinecarboxamide
https://huagongshe.com/reaction/1533129
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Di-tert-butyl dicarbonate | HCID 90495 | — |
| 反応物 | 3-Isopropylaniline | HCID 458679 | — |
| 反応物 | 6,7-Dimethoxy-4-piperazin-1-yl-quinazoline | HCID 2758484 | — |
| 触媒 | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 4-(6,7-Dimethoxy-4-quinazolinyl)-N-(3-isopropylphenyl)-1-piperazinecarboxamide | HCID 22707451 | 63% |
反応手順
To a solution of 2.05 g (9.39 mmol) of di-tert-butyl dicarbonate in 30 ml of dichloromethane was added 108 mg (0.88 mmol) of 4-(N,N-dimethylamino)pyridine. After the mixture was stirred at room temperature for 5 minutes, 1.26 ml (8.95 mmol) of 3-isopropylaniline was added thereto, followed by further stirring at room temperature for 30 minutes. To the reaction mixture was added 548 mg (2.00 mmol) of 6,7-dimethoxy-4-piperazinylquinazoline obtained by the method described in South African Patent No. 67 06512 (1968), followed by stirring at room temperature for 30 minutes. After the solvent was evaporated, the residue was purified by silica gel chromatography and recrystallized from ethyl acetate to give the desired compound as colorless crystals.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06207667B1 |
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| 出典データセット | uspto-grants-2001_03 |
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| ORD ID | ord-2adcde8e68624cd799b5ea6e4f02408c |
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| 出典メモ | uspto-grants-2001_03 |
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