Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2204738Generated: November 1, 2026

1,2-Dichloroethane → HCID 68060115, compound

https://huagongshe.com/reaction/2204738

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantHydrochloric AcidHCID 313—
ReactantLithium HydroxideHCID 3939—
ReactantDiisopropylethylamineHCID 81531—
ReactantHOAtHCID 181649—
Reactant4-AminopyridazineHCID 298492—
ReactantHCID 66611435HCID 66611435—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68060115HCID 68060115—

Reaction Steps

To a solution of methyl 2-{[(4-fluorophenyl)methyl]oxy}-4-(1-methyl-1H-pyrazol-4-yl)-5-(4-morpholinylmethyl)benzoate (may be prepared as described in Description 18; 144 mg, 0.33 mmol) in tetrahydrofuran (4 ml) was added lithium hydroxide (23.54 mg, 0.98 mmol) and water (1 ml). The mixture was stirred at room temperature for 18 hours then neutralised with 2M hydrochloric acid (0.79 ml, 1.59 mmol). The solvent was removed in vacuo and the residue redissolved in N,N-dimethylformamide (4 ml). Diisopropylethylamine (0.11 m, 0.66 mmol), 4-pyridazinamine (40.5 mg, 0.43 mmol), 1-hydroxy-7-azabenzotriazole (53.5 mg, 0.39 mmol) and EDC (94 mg, 0.49 mmol) were added and the solution was stirred for 3 hours. The solvent was removed in vacuo and the residue purified by MDAP to yield the title compound as a white solid. 57 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365551B2
Source datasetuspto-grants-2016_06
ORD IDord-5723953a1f144313b081368fe68739ac
Source noteuspto-grants-2016_06