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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1058834Generated: October 26, 2026

Dichloromethane → 4-[3-({1-[bis-(4-chlorophenyl)methyl]azetidin-3-ylidene}methane-sulfonylmethyl)phenyl]piperazine-1-carboxylic acid N-methylamide

https://huagongshe.com/reaction/1058834

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantMethyl IsocyanateHCID 12228—
Reactant1-[3-({1-[Bis-(4-chlorophenyl)methyl]azetidin-3-ylidene}methanesulfonylmethyl)phenyl]piperazineHCID 69635695—
SolventWaterHCID 962—
Product4-[3-({1-[bis-(4-chlorophenyl)methyl]azetidin-3-ylidene}methane-sulfonylmethyl)phenyl]piperazine-1-carboxylic acid N-methylamideHCID 69635622110.1%

Reaction Steps

2 cm3 of dichloromethane and then 11.5 mg of methyl isocyanate are successively added, at a temperature close to 20° C., to 54.25 mg of 1-[3-({1-[bis-(4-chlorophenyl)methyl]azetidin-3-ylidene}methanesulfonylmethyl)phenyl]piperazine. After stirring for 4 hours at a temperature close to 20° C., 0.05 cm3 of water is added to the mixture. After stirring for 15 minutes at the same temperature, the reaction medium is dried over magnesium sulfate, filtered on paper and concentrated to dryness under reduced pressure (1 kPa) at a temperature close to 40° C. 66 mg of 4-[3-({1-[bis-(4-chlorophenyl)methyl]azetidin-3-ylidene}methanesulfonylmethyl)phenyl]piperazine-1-carboxylic acid N-methylamide are thus obtained in the form of a beige lacquer [1H NMR spectrum (400 MHz, CDCl3), δ in ppm):

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06518264B2
Source datasetuspto-grants-2003_02
ORD IDord-6ede911f2eb04abaa80fa26c3fef9b07
Source noteuspto-grants-2003_02