HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 346417Generated: October 25, 2026
3-Morpholino-1-propanol → 4-[(3,4-Dichloro-6-fluorophenyl)amino]-7-[3-(4-morpholinyl)propoxy]-6-nitroquinazoline
https://huagongshe.com/reaction/346417
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Morpholino-1-propanol | HCID 199576 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 4-[(3,4-Dichloro-6-fluorophenyl)amino]-7-fluoro-6-nitroquinazoline | HCID 11176185 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-[(3,4-Dichloro-6-fluorophenyl)amino]-7-[3-(4-morpholinyl)propoxy]-6-nitroquinazoline | HCID 21080001 | 72% |
Reaction Steps
Sodium metal (5 equivalents) was added, under nitrogen atmosphere, to a solution of 3-(4-morpholinyl)-1-propanol (4 equivalents) in THF. The obtained suspension was stirred at 20° C. for two hours and was thereafter cannulated, under nitrogen atmosphere, into a solution of 4-[(3,4-dichloro-6-fluorophenyl)amino]-7-fluoro-6-nitroquinazoline. The reaction mixture was refluxed for 18 hours, the solvent was thereafter partially removed under reduced pressure and the residue was diluted with water and extracted with ethyl acetate. Drying the combined organic extracts, evaporation and silica gel chromatography (using a mixture of 20% MeOH/30% CH2Cl2/50% EtOAc as elute) gave 4-[(3,4-dichloro-6-fluorophenyl)amino]-7-[3-(4-morpholinyl)propoxy]-6-nitroquinazoline in 72% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07172749B2 |
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| Source dataset | uspto-grants-2007_02 |
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| ORD ID | ord-44f5507bc07f4cd99812ba644cbcabc3 |
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| Source note | uspto-grants-2007_02 |
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