Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602307Generated: October 31, 2026

3,5-Dimethylaniline → HCID 11964856, compound

https://huagongshe.com/reaction/602307

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-DimethylanilineHCID 7949—
ReactantEthyl AcetateHCID 8857—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 57971149HCID 57971149—
SolventDimethylformamideHCID 6228—
ProductHCID 11964856HCID 1196485641%

Reaction Steps

O-(7-Azabenzotriazole-1-yl)-N,N,N′,N′-tetrauroniumhexafluorophosphate (110 mg, 0.29 mmol) was added to a solution of 2-(2-aminopyrimidin-4-ylmethylthio)nicotinic acid (60 mg, 0.24 mmol, Reference Compound No. 12-1), 3,5-dimethylaniline (33 μL, 0.27 mmol) and N,N-diisopropylethylamine (0.93 μL, 0.53 mmol) in anhydrous N,N-dimethylformamide (1.0 mL) at room temperature, and the mixture was stirred for 18 hours. Ethyl acetate (30 mL) was added thereto, and then the whole was washed with saturated aqueous sodium hydrogencarbonate solution (50 mL) and brine (50 mL), then the organic layer was dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, the precipitated solid was filtered off, and washed with 50% diethylether-ethyl acetate solution. The solid was then dried at 60° C. under reduced pressure to give 35 mg of the target compound as a light brown solid (Yield: 41%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07906511B2
Source datasetuspto-grants-2011_03
ORD IDord-c9e54d16ba0c41198ebaff6802d1d479
Source noteuspto-grants-2011_03