HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → Quinazoline hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | 1-(3-Hydroxypropyl)pyrrolidin-2-one | HCID 566744 | — |
| Reactant | 4-(4-Bromo-2-fluoroanilino)7-hydroxy-6-methoxyquinoline | HCID 136411682 | — |
| Product | Quinazoline hydrochloride | HCID 21186983 | 67% |
Reaction Steps
Using a method analogous to that in Example 47, 4-(4-bromo-2-fluoroanilino)7-hydroxy-6-methoxyquinoline (146 mg, 0. mmol) in methylene chloride (5 ml) was treated with 1-(3hydroxypropyl)-2-pyrrolidinone (86 mg, 0.6 mmol), triphenylphosphine (314 mg, 1.2 mmol) and diethyl azodicarboxylate (209 mg, 1.2 mmol) and was purified and isolated to give 4-(4-bromo-2-fluoroanilino)-methoxy-73(oxopyrrolidin-1-yl)propoxy)quinazoline hydrochloride (140 mg, 67%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06897210B2 |
| Source dataset | uspto-grants-2005_05 |
| ORD ID | ord-33fcd66a73d04b5bb83ca849b9eeb3f2 |
| Source note | uspto-grants-2005_05 |