Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 578642생성일: 2026년 10월 25일
Phosphorus oxychloride → Methyl 4-{[4-chloro-3-(trifluoromethyl)benzyl]amino}-6-nitroquinazoline-8-carboxylate
https://huagongshe.com/reaction/578642
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Phosphorus oxychloride | HCID 24813 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | Benzenemethanamine, 4-chloro-3-(trifluoromethyl)- | HCID 485440 | — |
| 반응물 | Methyl 6-nitro-4-oxo-3,4-dihydroquinazoline-8-carboxylate | HCID 136278294 | — |
| 용매 | 1,2-Dichloroethane | HCID 11 | — |
| 생성물 | Methyl 4-{[4-chloro-3-(trifluoromethyl)benzyl]amino}-6-nitroquinazoline-8-carboxylate | HCID 66763565 | 46% |
반응 단계
To a solution of methyl 6-nitro-4-oxo-3,4-dihydroquinazoline-8-carboxylate (250 mg, 1.0 mmol) in 5 mL of anhydrous DCE, POCl3 (110 μL, 1.2 mmol, 1.2 equiv.) was added followed by DIPEA (870 μL, 5.0 mmol, 5.0 equiv.). The resulting mixture was stirred at 90° C. for 1 h. After cooling down to rt, 4-chloro-3-(trifluoromethyl)benzylamine (230 mg, 1.1 mmol, 1.1 equiv.) was added. The reaction mixture was stirred at 80° C. for 3 h. After work-up, the crude was purified by flash chromatography to yield the title compound in 46% yield. 1HNMR (in DMSO): 3.91 (s, 3H), 4.88 (d, J=5.9 Hz, 2H), 7.65-7.71 (m, 2H), 7.91 (s, 1H), 8.64 (s 1H), 8.68 (d, J=2.2 Hz, 1H), 9.49 (d, J=2.4 Hz, 1H), 9.70 (t, J=5.7 Hz, 1H). Mass: M+H+: 441.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09040560B2 |
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| 출처 데이터셋 | uspto-grants-2015_05 |
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| ORD ID | ord-1df950d5d7bb41a1a832ed26a83794cd |
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| 출처 메모 | uspto-grants-2015_05 |
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