Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1666936Generated: October 31, 2026

Hydrochloric Acid → 10H-Thieno[2,3-b][1,5]benzodiazepin-4-amine, 2-methyl-, hydrochloride (1:1)

https://huagongshe.com/reaction/1666936

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant5-Methyl-2-((2-nitrophenyl)amino)-3-thiophenecarbonitrileHCID 395460—
CatalystPalladiumHCID 23938—
SolventIsopropanolHCID 3776—
SolventEthyl AcetateHCID 8857—
Product10H-Thieno[2,3-b][1,5]benzodiazepin-4-amine, 2-methyl-, hydrochloride (1:1)HCID 135525650—

Reaction Conditions

Temperature81 °C

Reaction Steps

2-(2-Nitroanilino)-5-methylthiophene-3-carbonitrile (100 g) is taken in ethyl acetate (1000 ml). 5% Pd/C (15 g) is added and hydrogenated at 50° C. for 15 hours. Ethyl acetate is distilled off to get the solid. The solid is taken in isopropyl alcohol (500 ml), concentrated hydrochloric acid (102 ml) is added at room temperature and the mixture is heated up to 80-82° C. for 12 hours under stirring. The solution is cooled to precipitate the solid, filtered and dried under vacuum at 55-60° C. to give the title compound (80 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044196B2
Source datasetuspto-grants-2011_10
ORD IDord-65c313b7c3e44b2c886ea789c11ccc82
Source noteuspto-grants-2011_10