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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 353133생성일: 2026년 10월 25일

Di-tert-butyl dicarbonate → 4-(6,7-Dimethoxy-4-quinazolinyl)-N-(3-isopropylphenyl)-1-piperazinecarboxamide

https://huagongshe.com/reaction/353133

반응식

참여 물질

역할이름HCID투입량
반응물Di-tert-butyl dicarbonateHCID 90495—
반응물3-IsopropylanilineHCID 458679—
반응물6,7-Dimethoxy-4-piperazin-1-yl-quinazolineHCID 2758484—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DichloromethaneHCID 6344—
생성물4-(6,7-Dimethoxy-4-quinazolinyl)-N-(3-isopropylphenyl)-1-piperazinecarboxamideHCID 2270745163%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06750218B2
출처 데이터셋uspto-grants-2004_06
ORD IDord-bb64dae8372d4097a20658a543248991
출처 메모uspto-grants-2004_06