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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238117Generated: October 31, 2026

Sodium hydride → 7-Benzyloxy-4-(4-chloro-2,6-difluoroanilino)-6-methoxyquinazoline

https://huagongshe.com/reaction/238117

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant4-Chloro-2,6-DifluoroanilineHCID 1512518—
Reactant7-(Benzyloxy)-4-chloro-6-methoxyquinazolineHCID 10661998—
SolventDimethylformamideHCID 6228—
Product7-Benzyloxy-4-(4-chloro-2,6-difluoroanilino)-6-methoxyquinazolineHCID 1105902881.2%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642608B2
Source datasetuspto-grants-2014_02
ORD IDord-450a4bc8f3d04f2e9853550e9802ef09
Source noteuspto-grants-2014_02