HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 547209Generated: October 31, 2026
Triphenylphosphine → HCID 18753449, compound
https://huagongshe.com/reaction/547209
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | 3-(Methylamino)-1-propanol | HCID 10148986 | — |
| Reactant | 4-[(4-Bromo-2-fluorophenyl)amino]-6-methoxy-7-quinazolinol | HCID 135503852 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 18753449 | HCID 18753449 | 50.5% |
Reaction Steps
Diethyl azodicarboxylate (522 mg, 3 mmol) was added dropwise to a suspension of 4-(4-bromo-2-fluoroanilino)-7-hydroxy-6-methoxyquinazoline (364 mg, 1 mmol), (prepared as described for the starting material in Example 48), triphenylphosphine (786 mg, 3 mmol) and 3-methylamino-1-propanol (178 mg, 2 mmol), (J.Am.Chem.Soc., 1954, 76, 2789), in methylene chloride (4 ml) under nitrogen. The mixture was stirred for 1 hour at ambient temperature, neutral alumina (˜20 g) was added to the reaction mixture and the solvent was removed by evaporation. The powder was poured onto a column of neutral alumina and was eluted with a mixture of methylene chloride/methanol (95/5 followed by 90/10 and 80/20). The purified product was triturated with ether, collected by filtration, washed with ether and dried under vacuum to give 4-(4-bromo-2-fluoroanilino)-6-methoxy-7-(3-methylaminopropoxy)quinazoline (220 mg, 50%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | USRE042353E1 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-dc72f018b41643edaa411f585769fe69 |
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| Source note | uspto-grants-2011_05 |
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