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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1530688Generated: November 4, 2026

Sodium hydride → HCID 68312845, compound

https://huagongshe.com/reaction/1530688

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantHCID 12491978HCID 12491978—
ReactantHCID 68312705HCID 68312705—
SolventDimethylformamideHCID 6228—
ProductHCID 68312845HCID 6831284576.2%

Reaction Steps

To a suspension of 2-(2-isopropyl-5-methyl-2H-[1,2,4]triazol-3-yl)-4,5-dihydro-6-oxa-1,3a-diazabenzo[e]azulen-8-ol from Example 4 (300 mg, 0.922 mmol) in DMF (3 mL) was added sodium hydride (37 mg, 60% in oil, 0.925 mmol). The mixture was stirred at RT for 15 min, then a solution of 2-bromo-2-phenylmalonic acid diethyl ester (435 mg, 1.38 mmol) in DMF (0.5 mL) was added. The reaction mixture was stirred at RT for 30 min, and then at 90° C. for 2 h. The cooled reaction mixture was partitioned between water and EtOAc. The aqueous phase was extracted with EtOAc and the combined organic layers were washed with water, followed by brine, then dried (Na2SO4) and concentrated in vacuo. The resulting residue was purified by column chromatography (Si-PCC, gradient 2-10% MeOH in DCM) affording the title compound as a colourless gum (0.3933 g, 76%). LCMS (Method J): RT 3.73 min [M+H]+ 560

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09090628B2
Source datasetuspto-grants-2015_07
ORD IDord-780611dc580b4f1e8cdbec3befd9129e
Source noteuspto-grants-2015_07