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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1350412Generated: November 1, 2026

Dimethyl Sulfoxide → HCID 136005532, compound

https://huagongshe.com/reaction/1350412

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 58860729HCID 58860729—
Reactant10H-Thieno[2,3-b][1,5]benzodiazepin-4-amine, 2-methyl-, hydrochloride (1:1)HCID 135525650—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 136005532HCID 13600553250%

Reaction Conditions

Temperature105 °C

Reaction Steps

Combine 2-methyl-4H-3-thia-4,9-diaza-benzo[f]azulen-10-ylamine hydrochloride (829.8 mg, 3.12 mmol), (S)-2-[2-(3-chloro-phenyl)-ethyl]-piperazine (1.40 g, 6.24 mmol), N,N-diisopropylethylamine (403.6 mg, 3.12 mmol), DMSO (1.0 ml), and toluene (4.0 ml). Stir and heat the mixture at 105° C. After 48 hours, cool the mixture to ambient temperature and then dilute it with ethyl acetate and water. Remove the organic layer and wash it with 1N NaOH and brine. Dry (sodium sulfate) and concentrate the organic layer to residue. Purify the residue on silica gel using dichloromethane/methanol (95:5) to give 673.9 mg (50%) of the title compound as a brown foam: mp 68–74°, dec; mass spectrum (ES+): m/e=437.31.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07214673B2
Source datasetuspto-grants-2007_05
ORD IDord-54eb73e51bbd42a8af384804a39f8df3
Source noteuspto-grants-2007_05