HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453990Generated: November 1, 2026
Potassium Carbonate → 7-(3-(1,1-Dioxothiomorpholino)propoxy)-6-methoxy-4-(quinolin-7-yloxy)quinazoline
https://huagongshe.com/reaction/453990
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Chloro-7-(3-(1,1-dioxothiomorpholino)propoxy)-6-methoxyquinazoline | HCID 21936000 | — |
| Reactant | 7-Hydroxyquinoline | HCID 135426866 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 7-(3-(1,1-Dioxothiomorpholino)propoxy)-6-methoxy-4-(quinolin-7-yloxy)quinazoline | HCID 9870376 | 73% |
Reaction Steps
A mixture of 4-chloro-7-(3-(1,1-dioxothiomorpholino)propoxy)-6-methoxyquinazoline (220 mg, 0.57 mmol), potassium carbonate (106 mg, 0.77 mmol) and 7-hydroxyquinoline (111 mg, 0.76 mmol) in DMF (7.5 ml) was stirred at 100° C. for 5 hours then allowed to cool to ambient temperature. The reaction mixture was treated with 1M aqueous sodium hydroxide solution (40 ml) and stirred at ambient temperature for a few minutes. The crude solid was collected by filtration washing with water. The resultant solid was dissolved in dichloromethane (2 ml) and was filtered through phase separating paper. The filtrate was evaporated under vacuum to give a solid residue which was triturated with ether, filtered and dried to give 7-(3-(1,1-dioxothiomorpholino)propoxy)-6-methoxy-4-(quinolin-7-yloxy)quinazoline (205 mg, 73%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08492560B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-7ddb8060bdc544a5b9d8d4bb1b57115a |
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| Source note | uspto-grants-2013_07 |
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