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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1012161Generated: October 25, 2026

1,2-Dichloroethane → HCID 178522446, compound

https://huagongshe.com/reaction/1012161

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantTriethylamineHCID 8471—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant6-Chloropyridine-3,4-diamineHCID 817133—
ReactantHCID 178524951HCID 178524951—
SolventDimethylformamideHCID 6228—
ProductHCID 178522446HCID 1785224466.5%

Reaction Steps

A mixture of 4-(2,6-difluorobenzylamino)-1H-pyrazole-3-carboxylic acid (100 mg, 0.37 mmol) (Example 16D), 6-chloro-pyridine-3,4-diamine (54 mg, 0.37 mmol), EDC (72 mg, 0.40 mmol), HOBt (57.3 mg, 0.40 mmol) and Et3N (0.075 ml, 0.55 mmol) in DMF (20 ml) was stirred at ambient temperature for 48 h and then partitioned between EtOAc and saturated aqueous sodium bicarbonate and the organic portion dried (MgSO4), filtered and evaporated. The amide intermediate was dissolved in AcOH (3 ml), heated at reflux for 1 h, and then heated in the microwave (150 W) at 160° C. until the reaction was complete. The reaction mixture was allowed to cool, a solid crystallised out, which was filtered and then washed with petroleum ether and dried to give the required product (9 mg). (LC/MS: Rt 2.74, [M+H]+ 375)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977477B2
Source datasetuspto-grants-2011_07
ORD IDord-3cd9bfea20264e5cb6f277b84ad2b8a7
Source noteuspto-grants-2011_07