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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1863156Generated: October 31, 2026

Phenylacetyl chloride → 4,9-Dihydro-4-phenylacetyl-10H-thieno[3,4-b][1,5]benzodiazepin-10-one

https://huagongshe.com/reaction/1863156

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetyl chlorideHCID 7679—
Reactant4,9-dihydro-10H-thieno[3,4-b][1,5]benzodiazepin-10-oneHCID 12521641—
SolventBenzeneHCID 241—
Product4,9-Dihydro-4-phenylacetyl-10H-thieno[3,4-b][1,5]benzodiazepin-10-oneHCID 20392249—

Reaction Steps

A reaction mixture comprising 6.48 g. of 4,9-dihydro-10H-thieno[3,4-b][1,5]benzodiazepin-10-one and 25 g. of phenylacetyl chloride in 100 ml. of benzene is refluxed with stirring for 3 hours. The mixture is evaporated to an amber oil, combined with 100 ml. of ethanol and 6 ml. of 5 N sodium hydroxide and allowed to stand at room temperature for one hour. This solution is evaporated to an oily residue which is triturated with water and filtered, giving the desired product as pale pink crystals, mp. 165°-168° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04168269
Source datasetuspto-grants-1979_09
ORD IDord-bff9e9a0063c4c5f86a50e2699e56d32
Source noteuspto-grants-1979_09