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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1454993Generated: October 31, 2026

Potassium Carbonate → HCID 67307138, compound

https://huagongshe.com/reaction/1454993

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-(3-Bromophenyl)propan-1-olHCID 18785928—
ReactantHCID 60209555HCID 60209555—
SolventDichloromethaneHCID 6344—
ProductHCID 67307138HCID 6730713839.3%

Reaction Conditions

Temperature75 °C

Reaction Steps

A solution of 1.57 g (6.7 mmol) of 3-(3-bromophenyl)propan-1-ol, prepared in step 7.1., and 1.73 ml (10.1 mmol) of diisopropylethylamine in 38 ml of dichloromethane, cooled to 0° C., is admixed with 0.63 ml (8.14 mmol) of methanesulphonyl chloride. Stirring is continued in the cold for 0.5 hour and then at ambient temperature for 2 hours. The mixture is concentrated under reduced pressure and then the residue is suspended in 35 ml of acetonitrile. 1.34 g (5.35 mmol) of 2-(methylamino)-2-oxoethyl piperazine-1-carboxylate hydrochloride, prepared in accordance with Example 3.3., and 2.2 g (16 mmol) of potassium carbonate are added. The mixture is heated at 75° C. for 16 hours. After cooling to ambient temperature it is concentrated under reduced pressure and then the residue is taken up in water. It is extracted with ethyl acetate and dried over sodium sulphate. Following filtration, the organic phase is concentrated under reduced pressure. It is purified by chromatography on silica gel, eluting with a 98/2 mixture of dichloromethane and methanol. Crystallization from diisopropyl ether gives 0.84 g (2.10 mmol) of white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07482346B2
Source datasetuspto-grants-2009_01
ORD IDord-5aa8e18711e44008b5bf923148ad37bb
Source noteuspto-grants-2009_01