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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1744207Generated: October 31, 2026

2-(Trifluoromethyl)phenyl isothiocyanate → 4H-Pyrido(4',3':4,5)thieno(3,2-f)(1,2,4)triazolo(4,3-a)(1,4)diazepine-9(8H)-carbothioamide, 7,10-dihydro-6-(2-chlorophenyl)-1-methyl-N-(2-(trifluoromethyl)phenyl)-

https://huagongshe.com/reaction/1744207

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Trifluoromethyl)phenyl isothiocyanateHCID 737162—
ReactantHCID 14071251HCID 14071251—
Solvent1,2-DichloroethaneHCID 11—
Product4H-Pyrido(4',3':4,5)thieno(3,2-f)(1,2,4)triazolo(4,3-a)(1,4)diazepine-9(8H)-carbothioamide, 7,10-dihydro-6-(2-chlorophenyl)-1-methyl-N-(2-(trifluoromethyl)phenyl)-HCID 3076778—

Reaction Steps

A mixture containing 2-trifluoromethylphenyl isothiocyanate (0.82 g, 0.004 mol) and 6-(2-chlorophenyl)-7,8,9,10-tetrahydro-1-methyl-4H-pyrido[4′,3′;4,5]thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepine (1 g, 0.0027 mol) in 30 ml of 1,2-dichloroethane is agitated for 4 hours and at a temperature close to 20° C. Half the solvent is evaporated off with the rotary evaporator then 10 ml of ether is added. Agitation is carried out for 20 minutes at a temperature close to 20° C. followed by filtering on frit then washing with 20 ml of ether, with 20 ml of isopropyl ether and with 20 ml of isopentane. After drying under vacuum a cream coloured solid is obtained (1.21 g, 78%). Melting point: 190–192° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07015213B1
Source datasetuspto-grants-2006_03
ORD IDord-96f9d64d23b3477096b29c3d955a520b
Source noteuspto-grants-2006_03