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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Di-tert-butyl dicarbonate | HCID 90495 | — |
| 반응물 | 3-Isopropylaniline | HCID 458679 | — |
| 반응물 | 6,7-Dimethoxy-4-piperazin-1-yl-quinazoline | HCID 2758484 | — |
| 촉매 | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 4-(6,7-Dimethoxy-4-quinazolinyl)-N-(3-isopropylphenyl)-1-piperazinecarboxamide | HCID 22707451 | 63% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06750218B2 |
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| 출처 데이터셋 | uspto-grants-2004_06 |
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| ORD ID | ord-bb64dae8372d4097a20658a543248991 |
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| 출처 메모 | uspto-grants-2004_06 |
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