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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 131455Generated: October 25, 2026

Dimethyl Sulfoxide → (S)-7-Chloro-10-[3-(2-methoxy-ethyl)-piperazin-1-yl]-4H-3-thia-4,9-diaza-benzo[f]azulene

https://huagongshe.com/reaction/131455

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTolueneHCID 1140—
Reactant(S)-2-(2-Methoxyethyl)piperazineHCID 55287560—
Reactant7-Chloro-4H-3-thia-4,9-diaza-benzo[f]azulen-10-ylamine hydrochlorideHCID 136388576—
SolventEthyl AcetateHCID 8857—
Product(S)-7-Chloro-10-[3-(2-methoxy-ethyl)-piperazin-1-yl]-4H-3-thia-4,9-diaza-benzo[f]azuleneHCID 13543400436.2%

Reaction Conditions

Temperature105 °C

Reaction Steps

Combine 7-Chloro-4H-3-thia-4,9-diaza-benzo[f]azulen-10-ylamine hydrochloride (1.20 g, 4.19 mmol), (S)-2-(2-methoxy-ethyl)-piperazine (1.51 g, 10.48 mmol), DMSO (4.0 ml), and toluene (16.0 ml). Stir and heat the mixture at 105° C. After 24 hours, cool the mixture to ambient temperature and stir it for 16 hours. Dilute the mixture with ethyl acetate and wash the organic layer with 0.1N NaOH and brine. Dry (sodium sulfate) and concentrate the organic layer to residue. Purify the residue on silica gel using a gradient of dichloromethane to dichloromethane/methanol (90:10) to give 571.5 mg (36%) of an brown solid: mass spectrum (ion spray): m/z=377.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07384934B2
Source datasetuspto-grants-2008_06
ORD IDord-7d0f37f5ab52410993de3d9113428afc
Source noteuspto-grants-2008_06