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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1531301Generated: October 29, 2026

Dimethyl Sulfoxide → Dimethyl Sulfide

https://huagongshe.com/reaction/1531301

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantPyridineHCID 1049—
Reactant6-Methyl-4'-trifluoromethylbiphenyl-2-carboxylic acid chlorideHCID 11055639—
Reactant(R)-Methyl (5-amino-2,3-dihydro-1H-inden-2-yl)carbamateHCID 11413084—
SolventDichloromethaneHCID 6344—
ProductDimethyl SulfideHCID 1068—
Product(r)-6-Methyl-4'-trifluoromethylbiphenyl-2-carboxylic acid (2-methoxycarbonylaminoindan-5-yl)-amideHCID 9869236—

Reaction Steps

To an ice bath cooled solution of (R)-(5-aminoindan-2-yl)-carbamic acid methyl ester (9.5 g, 46.1 mmol), ([α]D=−26.29° (c=9.87 mg/mL, DMSO); mp 144-145° C.) and pyridine (4.48 mL, 55.5 mmol) in 200 mL of methylene chloride is added 6-methyl-4′-trifluoromethylbiphenyl-2-carboxylic acid chloride ( 80.5 mL of a 0.63 M solution in methylene chloride, 50.7 mmol). The reaction is stirred for 15 minutes at room temperature. The mixture is washed with 1N HCl, bicarbonate and brine. The organic layer is dried over magnesium sulfate, filtered, and concentrated under reduced pressure. The product is purified by crystallization from ethyl acetate/hexanes (1:2) to give (R)-6-methyl-4′-trifluoromethylbiphenyl-2-carboxylic acid (2-methoxycarbonylaminoindan-5-yl)-amide as a crystalline solid, mp 112-114° C. [α]D=−12.85°, c=11.36 mg/mL DMS.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06197798B1
Source datasetuspto-grants-2001_03
ORD IDord-993606a201e84e4a9ceb930785f13034
Source noteuspto-grants-2001_03