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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2100346Generated: November 1, 2026

2,6-Lutidine → HCID 57799150, compound

https://huagongshe.com/reaction/2100346

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-LutidineHCID 7937—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 18180195HCID 18180195—
Reactant1-[2-[(Trimethylsilyl)methoxy]ethyl]-1H-pyrazole-5-carboxylic acidHCID 67398926—
CatalystDimethylformamideHCID 6228—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
ProductHCID 57799150HCID 57799150—

Reaction Steps

Oxalyl chloride (0.17 ml, 1.9 mmol) was added to a slurry of 2-(2-trimethylsilanylmethoxy-ethyl)-2H-pyrazole-3-carboxylic acid) (Heterocycles (1992) 34 303-314), (428 mg, 1.76 mmol) in dichloromethane (15 ml), 1 drop of dimethylformamide was added and the reaction stirred at room temperature under N2 for 1 hour before concentrating in vacuo and azeotroping with dichloromethane. The resulting acid chloride was dissolved in 5 ml acetonitrile and added to a solution of 3-(2,5-dichloro-phenyl)pyrazine-2,6-diamine (Preparation 11, 300 mg, 1.18 mmol) in acetonitrile (15 ml) and 2,6-lutidine (0.21 ml, 1.8 mmol). The reaction was stirred at room temperature under N2 for 72 hours before concentrating in vacuo then partitioning between 50 ml ethyl acetate and 50 ml water. The organic layer was dried over MgSO4 and concentrated in vacuo to give a brown oil which was purified by column chromatography (ethyl acetate, heptane, 1:2) to give 52 mg of the title product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07572797B2
Source datasetuspto-grants-2009_08
ORD IDord-33a657c2ac13400dadb592821632972f
Source noteuspto-grants-2009_08