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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 131416Generated: October 26, 2026

Dimethyl Sulfoxide → (S)-3-Methyl-11-[3-(2-methoxy-ethyl)-piperazin-1-yl]-5H-dibenzo[b,e][1,4]diazepine

https://huagongshe.com/reaction/131416

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-methyl-5H-dibenzo[b,e][1,4]diazepin-1-ylamine hydrochlorideHCID 21093525—
Reactant(S)-2-(2-Methoxyethyl)piperazineHCID 55287560—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product(S)-3-Methyl-11-[3-(2-methoxy-ethyl)-piperazin-1-yl]-5H-dibenzo[b,e][1,4]diazepineHCID 5862600948%

Reaction Conditions

Temperature110 °C

Reaction Steps

Combine 3-methyl-5H-dibenzo[b,e][1,4]diazepin-1-ylamine hydrochloride (400.0 mg, 1.54 mmol), (S)-2-(2-methoxy-ethyl)-piperazine (444.2 mg, 3.08 mmol), N,N-diisopropylethylamine (199.0 mg, 1.54 mmol), DMSO (0.7 ml), and toluene (2.8 ml) and stir and heat the mixture at 110° C. After 48 hours, cool the mixture to ambient temperature and dilute with ethyl acetate. 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 dichloromethane/methanol (90:10) to give 257.1 mg (48%) of a yellow foam: mp=64° C. dec; mass spectrum (ion spray): m/z =433.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07384934B2
Source datasetuspto-grants-2008_06
ORD IDord-799c2269df80402989ecd0378d73e031
Source noteuspto-grants-2008_06