HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454268Generated: October 27, 2026
Potassium Carbonate → 6-Methoxy-4-(3-methylindol-5-yloxy)-7-(2-morpholinoethoxy)quinazoline
https://huagongshe.com/reaction/454268
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Morpholine, 4-(2-chloroethyl)-, hydrochloride (1:1) | HCID 77210 | — |
| Reactant | 7-Hydroxy-6-methoxy-4-(3-methylindol-5-yloxy)quinazoline | HCID 135763115 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-Methoxy-4-(3-methylindol-5-yloxy)-7-(2-morpholinoethoxy)quinazoline | HCID 22030931 | 47.1% |
Reaction Steps
A mixture of 7-hydroxy-6-methoxy-4-(3-methylindol-5-yloxy)quinazoline (800 mg, 2.49 mmol), (prepared as described for the starting material in Example 271), potassium carbonate (1.031 g, 7.47 mmol) and 4-(2-chloroethyl)morpholine hydrochloride (510 mg, 2.74 mmol) in DMF (25 ml) was stirred at 80° C. for 2 hours and allowed to cool to ambient temperature. The reaction mixture was filtered and the filtrate removed in vacuo. The residue was purified by silica column chromatography, gradient elution (dichloromethane, 5% methanol/95% dichloromethane, methanol/dichloromethane/0.880 saturated aqueous ammonia (100/8/1)) and the product recrystallised from ethanol to give 6-methoxy-4-(3-methylindol-5-yloxy)-7-(2-morpholinoethoxy)quinazoline (510 mg, 47%).
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-cfe58e68751f4859bf60861e084f1a52 |
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| Source note | uspto-grants-2013_07 |
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