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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1437115Generated: October 31, 2026

Benzyl Bromide → 9-Benzyl-2-chloro-8,9-dihydro-5,7,7-trimethyl-5H-pyrimido[4,5-b][1,4]diazepin-6(7H)-one

https://huagongshe.com/reaction/1437115

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantHCID 57940470HCID 57940470—
SolventDimethylacetamideHCID 31374—
Product9-Benzyl-2-chloro-8,9-dihydro-5,7,7-trimethyl-5H-pyrimido[4,5-b][1,4]diazepin-6(7H)-oneHCID 5794050091%

Reaction Steps

2-Chloro-8,9-dihydro-5,7,7-trimethyl-5H-pyrimido[4,5-b][1,4]diazepin-6(7H)-one (50 mg, 0.21 mmol) and benzylbromide (30 μl, 0.25 mmol) in DMA (0.5 ml) was treated with sodium hydride 60% oil dispersion (9 mg, 0.23 mmol) at room temperature. The mixture was stirred at room temperature for 5 hours. The reaction mixture was concentrated under reduced pressure. The residue was purified by column chromatography (50% EtOAc in hexanes, loaded on silica, ˜50 mL silica) to give the title compound as a white solid (63 mg, 91%). NMR DMSO D6 1.00 (6H, s), 3.22 (3H, s), 3.53 (2H, s), 4.91 (2H, s), 7.28-7.39 (5H, m), 8.12 (1H, s); MS (ES+) 331.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07622463B2
Source datasetuspto-grants-2009_11
ORD IDord-b1206646d0cb4e50a7ee2e1a331508bf
Source noteuspto-grants-2009_11