HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2068038Generated: October 31, 2026
Potassium Carbonate → 4-(7-Azaindol-5-yloxy)-6-methoxy-7-(3-(4-methylsulphonylpiperazin-1-yl)propoxy)quinazoline
https://huagongshe.com/reaction/2068038
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1H-Pyrrolo[2,3-b]pyridin-5-ol | HCID 22030722 | — |
| Reactant | 4-Chloro-6-methoxy-7-(3-(4-methylsulphonylpiperazin-1-yl)propoxy)quinazoline | HCID 86618098 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(7-Azaindol-5-yloxy)-6-methoxy-7-(3-(4-methylsulphonylpiperazin-1-yl)propoxy)quinazoline | HCID 10174598 | 45% |
Reaction Steps
A suspension of 4-chloro-6-methoxy-7-(3-(4-methylsulphonylpiperazin-1-yl)propoxy)quinazoline (0.25 g, 0.66 mmol), 5-hydroxy-7-azaindole (0.089 g, 0.663 mmol), (prepared as described for the starting material in Example 2), and potassium carbonate (0.091 g, 0.66 mmol) in DMF (3 ml) was stirred at 85° C. for 3 hours. The mixture was filtered and the filtrate was purified by preparative LCtMS eluting with acetonitrile/water (containing 1% acetic acid). The fractions containing the expected product were combined and evaporated. The residue was dissolved in methylene chloride and washed with 0.5N aqueous ammonia followed by brine, dried (MgSO4) and evaporated. The residue was triturated under diethyl ether, filtered and dried under vacuum to give 4-(7-azaindol-5-yloxy)-6-methoxy-7-(3-(4-methylsulphonylpiperazin-1-yl)propoxy)quinazoline (0.138 g, 45%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08293902B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-0f84e3198ab94000a7e0e2a4df767612 |
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| Source note | uspto-grants-2012_10 |
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