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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 355530Generated: October 30, 2026

Triethylorthoaceate → 8-Chloro-6-(2-fluorophenyl)-3a,4-dihydro-1-methyl-3H-imidazo[1,5-a][1,4]benzodiazepine-5-oxide

https://huagongshe.com/reaction/355530

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylorthoaceateHCID 21875354—
ReactantHCID 178510496HCID 178510496—
SolventAcetonitrileHCID 6342—
Product8-Chloro-6-(2-fluorophenyl)-3a,4-dihydro-1-methyl-3H-imidazo[1,5-a][1,4]benzodiazepine-5-oxideHCID 11824106—

Reaction Steps

A slurry of 7-chloro-5-(2-fluorophenyl)-2,3-dihydro-1H-1,4-benzodiazepine-2-methanamine-4-oxide oxalate salt (VIII, EXAMPLE 6, 35 g, 85 mmol) and triethylorthoacetate (23.5 ml, 128 mmol) in acetonitrile (175 ml) is stirred at reflux for 2 hr during which time the 7-chloro-5-(2-fluorophenyl)-2,3-dihydro-1H-1,4-benzodiazepine-2-methanamine-4-oxide (VIII) dissolves and ethanol/acetonitrile (about 75 ml) is removed by distillation under ordinary pressure. TLC and HPLC analysis shows the reaction is complete. The temperature is adjusted to 40° and methyl t-butyl ether (175 ml) is added dropwise over about 1 hr. The resulting slurry is cooled to 5°, stirred 1 hr, the solids are collected and are washed with t-butyl ether. The product is dried in the vacuum oven at 35° to give the title compound as the oxalate salt, mp=178°-180°; TLC (methylene chloride/methanol/ammonium hydroxide, 90/10/1) Rf =0.28.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05831089
Source datasetuspto-grants-1998_11
ORD IDord-bc89a8ad53ff4743a73b745807be07a1
Source noteuspto-grants-1998_11