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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17375Generated: October 29, 2026

Dimethyl Sulfoxide → 4-Cyano-N,N,5-trimethyl-7-[(3R)-3-(dimethylamino)pyrrolidin-1-yl]-6-phenyl-1,3-benzoxazole-2-carboxamide

https://huagongshe.com/reaction/17375

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
Reactant(3R)-(+)-3-(Methylamino)pyrrolidineHCID 10261056—
Reactant4-Cyano-7-fluoro-N,N,5-trimethyl-6-phenyl-1,3-benzoxazole-2-carboxamideHCID 51042335—
SolventSodium chloride; waterHCID 57417360—
Product4-Cyano-N,N,5-trimethyl-7-[(3R)-3-(dimethylamino)pyrrolidin-1-yl]-6-phenyl-1,3-benzoxazole-2-carboxamideHCID 6858538923%

Reaction Steps

Under nitrogen atmosphere, a dimethyl sulfoxide (2 ml) solution of (3R)-3-methylaminopyrrolidine (85 μl, 660 μmol) was added at 150° C. to a dimethyl sulfoxide (11 ml) solution of 4-cyano-7-fluoro-N,N,5-trimethyl-6-phenyl-1,3-benzoxazole-2-carboxamide (I-114) (180 mg, 557 μmol) and triethylamine (101 μl, 724 μmol), followed by stirring at the same temperature for 30 minutes. After cooling, saturated brine was added to the reaction liquid, and the reaction liquid was extracted with chloroform. Next, the combined organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, filtered, and the filtrate was concentrated under reduced pressure. The resulting residue was subjected to preparative silica gel column chromatography. The eluate with chloroform/methanol (10:1, v/v) gave the entitled compound (53 mg, 23%) as a white amorphous substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737166B2
Source datasetuspto-grants-2010_06
ORD IDord-8a6762ba6ab24b5cabc718b66a9cf14a
Source noteuspto-grants-2010_06