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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1012168Generated: October 31, 2026

1,2-Dichloroethane → HCID 178486895, compound

https://huagongshe.com/reaction/1012168

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant4-Methoxy-5-(4-methyl-piperidin-1-ylmethoxy)-benzene-1,2-diamineHCID 67106286—
ReactantHCID 178490649HCID 178490649—
SolventDimethylformamideHCID 6228—
ProductHCID 178486895HCID 1784868950.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 4-(5-Chloro-2-methoxy-benzoylamino)-1H-pyrazole-3-carboxylic acid (0.22 g, 0.745 mmol), 4-Methoxy-5-(4-methyl-piperidin-1-ylmethoxy)-benzene-1,2-diamine (0.2 g, 0.745 mmol), EDC (0.173 g, 0.89 mmol) and HOBt (0.122 g, 0.89 mmol) in DMF (20 ml) was stirred at 80° C. for 1 hour then at ambient temperature for 16 hours and then reduced in vacuo. The residue was partitioned between EtOAc and saturated bicarbonate, the organic portion was washed with brine and dried (MgSO4), filtered and evaporated. The amide intermediate (150 mg), (LC/MS (acidic method): Rt 2.13, [M+H]+ 543) was dissolved in AcOH (5 ml) then heated at reflux for 4 hours. The reaction mixture was allowed to cool, reduced in vacuo, residue purified by preparative TLC to yield 5-Chloro-2-methoxy-N-{3-[6-methoxy-5-(1-methyl-piperidin-4-ylmethoxy)-1H-benzimidazol-2-yl-]1H-pyrazol-4-yl}-benzamide (2 mg). (LC/MS (acidic method): Rt 2.25, [M+H]+ 525)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977477B2
Source datasetuspto-grants-2011_07
ORD IDord-9346cdf64545492589d5db45ab53d4f0
Source noteuspto-grants-2011_07