HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454281Generated: October 30, 2026
1-(3-Aminopropyl)-4-methylpiperazine → HCID 54524703, compound
https://huagongshe.com/reaction/454281
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-(3-Aminopropyl)-4-methylpiperazine | HCID 78328 | — |
| Reactant | (2R)-6-methoxy-4-(3-methylindol-5-yloxy)-7-(oxiran-2-ylmethoxy)quinazoline | HCID 54069082 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 54524703 | HCID 54524703 | 31% |
Reaction Steps
A mixture of (2R)-6-methoxy-4-(3-methylindol-5-yloxy)-7-(oxiran-2-ylmethoxy)quinazoline (100 mg, 0.28 mmol), (prepared as described in Example 278), and 1-(3-aminopropyl)-4-methylpiperazine (132 mg, 0.84 mmol) in DMF (5 ml) was heated to 70° C. for 3 hours. The solvents were removed in vacuo and the residue taken up in dichloromethane. This was washed with water, dried (MgSO4), filtered and evaporated. The residue was purified by silica column chromatography using gradient elution (dichloromethane, 5% methanol/95% dichloromethane, 20% methanolic ammonia (7M)/80% dichloromethane) to give (2R)-7-(2-hydroxy-3-(3-(4-methylpiperazin-1-yl)propylamino)propoxy)-6-methoxy-4-(3-methylindol-5-yloxy)quinazoline (44 mg, 31%).
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-9a592a97bdba4ae0b35de335e8918164 |
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| Source note | uspto-grants-2013_07 |
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