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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1645155Generated: October 30, 2026

Sodium methanesulfinate → [(R)-4-(3-methanesulfonyl-5-trifluoromethyl-benzenesulfonylamino)-4,5,6,7-tetrahydro-indazol-1-yl]-acetic acid ethyl ester

https://huagongshe.com/reaction/1645155

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium methanesulfinateHCID 2733271—
ReactantL-Proline sodium saltHCID 23678551—
ReactantHCID 44611775HCID 44611775—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product[(R)-4-(3-methanesulfonyl-5-trifluoromethyl-benzenesulfonylamino)-4,5,6,7-tetrahydro-indazol-1-yl]-acetic acid ethyl esterHCID 5915295551.1%

Reaction Conditions

Temperature150 °C

Reaction Steps

[(R)-4-(3-Bromo-5-trifluoromethyl-benzenesulfonylamino)-4,5,6,7-tetrahydro-indazol-1-yl]-acetic acid ethyl ester (118.0 mg, 0.20 mmol), methanesulfinic acid sodium salt (24.5 mg, 0.24 mmol), copper(I) iodide (4.0 mg, 0.02 mmol) and L-proline sodium salt (3.2 mg, 0.04 mmol) were dissolved in dimethyl sulfoxide (1.5 mL) and water (0.3 mL). The mixture was heated in a microwave oven at 150° C. for 30 minutes. The resulting mixture was diluted with water and extracted with ethyl acetate. The organic layer was washed with brine, dried over sodium sulfate, concentrated and purified by column chromatography (gradient elution, 0-5% methanol in dichloromethane) to afford [(R)-4-(3-methanesulfonyl-5-trifluoromethyl-benzenesulfonylamino)-4,5,6,7-tetrahydro-indazol-1-yl]-acetic acid ethyl ester (52.0 mg, 51.1%) as a white solid. MS calcd. for C19H22F3N3O6S2 509, obsd. (ESI+) [(M+H)+] 510.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124641B2
Source datasetuspto-grants-2012_02
ORD IDord-cf884dbf029d4dd39b18463c1d68e255
Source noteuspto-grants-2012_02