HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384677Generated: October 31, 2026
Dimethylformamide → 4-Chloro-6-methoxy-7-(2-(imidazol-1-yl)ethoxy)quinazoline
https://huagongshe.com/reaction/1384677
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 7-(2-(Imidazol-1-yl)ethoxy)-6-methoxy-3,4-dihydroquinazolin-4-one | HCID 135490844 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-Chloro-6-methoxy-7-(2-(imidazol-1-yl)ethoxy)quinazoline | HCID 11141261 | 59% |
Reaction Steps
A mixture of 7-(2-(imidazol-1-yl)ethoxy)-6-methoxy-3,4-dihydroquinazolin-4-one (412 mg, 1.44 mmol), thionyl chloride (5 ml) and DMF (0.2 ml) was heated at reflux for 1hour. The mixture was diluted with toluene and the volatiles were removed by evaporation. The residue was suspended in methylene chloride, cooled to 0° C. and aqueous sodium hydrogen carbonate solution was added. The resulting precipitate was collected by filtration and dried under vacuum to give 4-chloro-7-(2-(imidazol-1-yl)ethoxy)-6-methoxyquinazoline (258 mg, 59%). 1H NMR Spectrum: (DMSOd6) 4.01(s, 3H); 4.47(m, 2H); 4.53(m, 2H); 6.89(s, 1H); 7.27(s, 1H); 7.41(s, 1H); 7.49(s, 1H); 7.70(s, 1H); 8.88(s, 1H) MS-ESI: 327 [MNa]+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06258951B1 |
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| Source dataset | uspto-grants-2001_07 |
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| ORD ID | ord-8bb8b6d782fe4eeb9270facfde0febc8 |
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| Source note | uspto-grants-2001_07 |
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