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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2044109Generated: November 3, 2026

Sodium hydride → 7-bromo-4-(pyrimidin-2-ylmethyl)-3,4-dihydrobenzo[f][1,4]oxazepin-5(2H)-one

https://huagongshe.com/reaction/2044109

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2-(Chloromethyl)pyrimidine hydrochlorideHCID 20025606—
Reactant7-Bromo-2,3,4,5-tetrahydro-1,4-benzoxazepin-5-oneHCID 60124972—
SolventDimethylformamideHCID 6228—
Product7-bromo-4-(pyrimidin-2-ylmethyl)-3,4-dihydrobenzo[f][1,4]oxazepin-5(2H)-oneHCID 71183408—

Reaction Steps

7-Bromo-3,4-dihydrobenzo[f][1,4]oxazepin-5(2H)-one (1.0 g, 4.13 mmol) was dissolved in DMF (10 ml) cooled down in a ice/water bath and treated with sodium hydride (60% dispersion) (363 mg, 9.08 mmol) portion wise. After 10 min a solution of 2-(chloromethyl)pyrimidine hydrochloride (813 mg, 4.96 mmol) in DMF (4 ml) was added, the reaction mixture warmed up to room temperature and quenched with 12 mL of water after it was complete. The reaction mixture was extracted with EtOAc and water and the organic phase was dried, evaporated and purified by silica gel chromatography (95% DCM/MeOH) to afford 7-bromo-4-(pyrimidin-2-ylmethyl)-3,4-dihydrobenzo[f][1,4]oxazepin-5(2H)-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586732B2
Source datasetuspto-grants-2013_11
ORD IDord-ba9207d4e0e54783a6959b39ea34485a
Source noteuspto-grants-2013_11