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HRID 353133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/353133

反応式

関与物質

役割名称HCID仕込み量
反応物Di-tert-butyl dicarbonateHCID 90495—
反応物3-IsopropylanilineHCID 458679—
反応物6,7-Dimethoxy-4-piperazin-1-yl-quinazolineHCID 2758484—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒DichloromethaneHCID 6344—
生成物4-(6,7-Dimethoxy-4-quinazolinyl)-N-(3-isopropylphenyl)-1-piperazinecarboxamideHCID 2270745163%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US06750218B2
出典データセットuspto-grants-2004_06
ORD IDord-bb64dae8372d4097a20658a543248991
出典メモuspto-grants-2004_06