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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 869164Generated: October 25, 2026

Diisopropylethylamine → 6-Chloro-3-(2-(4-fluorophenyl)-2-methylpropylamino)pyridazine-4-carboxamide

https://huagongshe.com/reaction/869164

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant3,6-Dichloropyridazine-4-carboxamideHCID 262049—
Reactant2-(4-Fluorophenyl)-2-methylpropan-1-amineHCID 21251023—
Reactant6-Chloro-N-(2-(4-fluorophenyl)-2-methylpropyl)-5-methylpyridazin-3-amineHCID 86686132—
SolventAcetonitrileHCID 6342—
Product6-Chloro-3-(2-(4-fluorophenyl)-2-methylpropylamino)pyridazine-4-carboxamideHCID 8668613378%

Reaction Steps

Using a similar procedure as was used for 6-chloro-N-(2-(4-fluorophenyl)-2-methylpropyl)-5-methylpyridazin-3-amine in example 14, 3,6-dichloropyridazine-4-carboxamide (2.6 g, 13 mmol, 1.0 equiv), (2-(4-fluorophenyl)-2-methylpropan-1-amine (2.5 g, 15 mmol, 1.1 equiv), and diisopropylethylamine (2.8 mL, 16 mmol, 1.2 equiv) in CH3CN (54 mL) was heated at 60-90° C. for 48 hours. The product was purified over silica gel with 100% EtOAc to give the desired product (3.4 g, 78%) as a yellow foamy solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969346B2
Source datasetuspto-grants-2015_03
ORD IDord-9775c6bde164473aa93b86c9935c1de6
Source noteuspto-grants-2015_03