Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598522Generated: October 25, 2026

Sodium Bicarbonate → [(r)-3-(5,6-Difluoro-benzothiazol-2-ylamino)-pyrrolidin-1-yl]-(5-methyl-2-trifluoromethyl-phenyl)-methanone

https://huagongshe.com/reaction/598522

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant5,6-Difluoro-2-(methylsulfinyl)benzo[d]thiazoleHCID 57748938—
Reactant((R)-3-Amino-pyrrolidin-1-yl)-(5-methyl-2-trifluoromethyl-phenyl)-methanoneHCID 57748952—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product[(r)-3-(5,6-Difluoro-benzothiazol-2-ylamino)-pyrrolidin-1-yl]-(5-methyl-2-trifluoromethyl-phenyl)-methanoneHCID 4264161747.6%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 30 mg (0.129 mmol) rac-5,6-difluoro-2-methanesulfinyl-benzothiazole and 70.3 mg (0.258 mmol) ((R)-3-Amino-pyrrolidin-1-yl)-(5-methyl-2-trifluoromethyl-phenyl)-methanone (intermediate 13) in 540 μL dimethyl sulfoxide was heated in a 100° C. oil-bath for 4 h. The solution was cooled to room temperature, diluted with water and basified with a saturated NaHCO3 solution. The mixture was stirred for 1 h. The solid was filtered, washed with water and dissolved in dichloromethane. The solution was dried over Na2SO4, filtered and concentrated in vacuo. The crude compound was purified with flash column chromatography on silica eluting with a gradient formed from n-heptane and ethyl acetate to provide 27 mg (47.6%) of the title compound as a white solid. MS(m/e): 442.2 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897627B2
Source datasetuspto-grants-2011_03
ORD IDord-cfd520eb60e74003b6fef6c9257ca90f
Source noteuspto-grants-2011_03