Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515233Generated: October 29, 2026

N-methyl-2-pyrrolidone → HCID 68245104, compound

https://huagongshe.com/reaction/515233

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-methyl-2-pyrrolidoneHCID 13387—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 86687903HCID 86687903—
SolventMethanolHCID 887—
ProductHCID 68245104HCID 68245104—

Reaction Steps

To a vial was added 1-[(2,2-difluorocyclopropyl)methyl]-3-methyl-5-(3-piperidin-4-ylphenyl)-1,3-dihydro[1,2,5]thiadiazolo[3,4-b]pyridine 2,2-dioxide (31-3) (0.030 g, 0.064 mmol), NMP (1 mL), DIPEA (0.060 mL, 0.344 mmol), and finally methanesulfonyl chloride (0.0374 mL, 0.480 mmol). The reaction mixture was then permitted to stir at room temperature for 1 hour. The crude reaction mixture was then diluted with methanol, then filtered. Purification of crude reaction mixture by reverse phase chromatography (Waters Sunfire MSC18, 10% acetonitrile/0.1% trifluoroacetic acid/water→100% acetonitrile/0.1% trifluoroacetic acid/water) to give 1-[(2,2-difluorocyclopropyl)methyl]-3-methyl-5-{3-[1-(methylsulfonyl)piperidin-4-yl]phenyl}-1,3-dihydro[1,2,5]thiadiazolo[3,4-b]pyridine 2,2-dioxide (31-4) as a tan solid. HRMS (M+H)+: observed=513.1430, calculated=513.1436.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108937B2
Source datasetuspto-grants-2015_08
ORD IDord-0dd4d7d3697849629e32f68b64059ba2
Source noteuspto-grants-2015_08