Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522305Generated: October 29, 2026

Dimethylformamide → HCID 117899577, compound

https://huagongshe.com/reaction/522305

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantIsobutylene oxideHCID 11208—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 117899560HCID 117899560—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 117899577HCID 117899577—

Reaction Conditions

Temperature60 °C

Reaction Steps

Isobutylene oxide (38 μL) and N,N-diisopropylethylamine (73 μL) were added to a solution of 7-methyl-4-[6-{[1-(piperidin-4-yl carbonyl)piperidin-4-yl]methoxy}-5-(trifluoromethyl)pyridin-3-yl]-7H-pyrrolo[2,3-d]pyrimidine-2-carbonitrile monohydrochloride (120 mg) in EtOH (2.4 mL)-DMF (0.5 mL) at room temperature, and the mixture was stirred at 60° C. overnight. The reaction mixture was cooled to room temperature, and EtAOc and water were added thereto. Extraction was performed on the mixture using EtOAc, and the extract was washed with saturated brine. The organic layer was dried over MgSO4 and filtered, and the filtrate was concentrated under reduced pressure. The residue was purified by basic silica gel column chromatography (Hex:CHCl3=70:30 to 20:80), whereby 4-{6-[(1-{[1-(2-hydroxy-2-methylpropyl)piperidin-4-yl]carbonyl}piperidin-4-yl)methoxy]-5-(trifluoromethyl)pyridin-3-yl}-7-methyl-7H-pyrrolo[2,3-d]pyrimidine-2-carbonitrile (93 mg) was obtained as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09328118B2
Source datasetuspto-grants-2016_05
ORD IDord-27f43812e58b4685b9173e47cd584ea9
Source noteuspto-grants-2016_05