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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1350512Generated: October 31, 2026

Dimethyl Sulfoxide → 11-{(S)-3-[2-(3-Fluoro-phenyl)-ethyl]-piperazin-1-yl}-3-methyl-5H-dibenzo[b,e][1,4]diazepine

https://huagongshe.com/reaction/1350512

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-(3-Fluoro-phenyl)-ethyl)-piperazineHCID 21093648—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product11-{(S)-3-[2-(3-Fluoro-phenyl)-ethyl]-piperazin-1-yl}-3-methyl-5H-dibenzo[b,e][1,4]diazepineHCID 5886072066.3%

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-(3-Fluoro-phenyl)-ethyl]-piperazine (641.5 mg, 3.08 mmol), N,N-diisopropylethylamine (199.0 mg, 1.54 mmol), DMSO (0.7 ml), and toluene (2.8 ml). Stir and heat the mixture at 110° C. After 64 hours, cool the mixture to ambient temperature and then dilute it with ethyl acetate. Wash the organic layer with 0.1 N 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 423.2 mg (66%) of a tan foam: mp 81°, dec; mass spectrum (ion spray): m/z 415.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07214673B2
Source datasetuspto-grants-2007_05
ORD IDord-f5bdfd117ce349e2bd6c4dc66c901cbc
Source noteuspto-grants-2007_05