HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → 7-Benzyloxy-4-(4-chloro-2,6-difluoroanilino)-6-methoxyquinazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Chloro-2,6-Difluoroaniline | HCID 1512518 | — |
| Reactant | 7-(Benzyloxy)-4-chloro-6-methoxyquinazoline | HCID 10661998 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 7-Benzyloxy-4-(4-chloro-2,6-difluoroanilino)-6-methoxyquinazoline | HCID 11059028 | 81.2% |
Reaction Steps
Using an analogous procedure to that described for the preparation of the starting material in Example 9, 7-benzyloxy-4-chloro-6-methoxyquinazoline (184 mg, 0.61 mmol), (prepared, for example, as described in WO 97/22596, Example 1, but the free base was generated prior to use), was reacted with 4-chloro-2,6-difluoroaniline (200 mg, 1.22 mmol) in the presence of sodium hydride (60%, 87 mg, 1.4 mmol) in DMF (8 ml) to give 7-benzyloxy-4-(4-chloro-2,6-difluoroanilino)-6-methoxyquinazoline (212 mg, 74%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07173038B1 |
| Source dataset | uspto-grants-2007_02 |
| ORD ID | ord-6b0186541e394a28af3f1d08396f1e91 |
| Source note | uspto-grants-2007_02 |