참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Mecloqualone | HCID 9567 | — |
| 반응물 | Dimethylformamide dimethyl acetal | HCID 78373 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 3-(2-Chloro-phenyl)-2-(2-dimethylamino-vinyl)-3,4-dihydro-quinazolin-4-one | HCID 53689769 | 62.4% |
반응 단계
A mixture of 3-(2-chloro-phenyl)-2-methyl-3,4-dihydro-quinazolin-4-one (1.0 g, 3.69 mmol) and dimethylformamide dimethyl acetal (0.64 mL, 4.8 mmol) in dimethylformamide (4 mL) was heated to 140° C. for 24 hours. Additional dimethylformamide dimethyl acetal (0.32 mL, 2.4 mmol) was added and heating was continued for an additional 24 hours. The reaction was cooled to ambient temperature and concentrated at reduced pressure (60° C. bath temperature). The dark residue was triturated with methanol and the pale orange solid which formed was collected and dried to give 0.75 g (62%) of 3-(2-chloro-phenyl)-2-(2-dimethylamino-vinyl)-3,4-dihydro-quinazolin-4-one which had: mp 228-230° C.; 1H 1H NMR δ 8.19 (d, J=8 Hz, 1 H), 7.91 (d, J=12.3 Hz, 1 H), 7.71-7.18 (m, 7 H), 4.10 (d, J=12.3 Hz, 1 H), 2.81 (br s, 6 H). Analysis calculated for C18H16ClN3O: C, 66.36; H, 4.95; N, 12.90. Found: C, 66.20; H, 5.03; N, 12.79.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06921764B2 |
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| 출처 데이터셋 | uspto-grants-2005_07 |
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| ORD ID | ord-9ec17971598e4b4e8f829fb8df34cf1d |
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| 출처 메모 | uspto-grants-2005_07 |
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