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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 388396Generated: October 29, 2026

Diisopropylethylamine → HCID 44462841, compound

https://huagongshe.com/reaction/388396

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant6-(trifluoromethyl)pyridazine-3-carboxylic acidHCID 58126820—
Reactant1H-Indole-5-methanamine, 2-(trifluoromethyl)-, hydrochloride (1:1)HCID 66909363—
SolventAcetonitrileHCID 6342—
ProductHCID 44462841HCID 44462841—

Reaction Steps

A solution of 6-(trifluoromethyl)-3-pyridazinecarboxylic acid (Intermediate 9, 60 mg, 0.312 mmol), HATU (131 mg, 0.344 mmol) and DIPEA (0.164 ml, 0.937 mmol) in acetonitrile (3 ml) was stirred at room temperature under argon for 15 mins and then treated with {[2-(trifluoromethyl)-1H-indol-5-yl]methyl}amine hydrochloride (Intermediate 5, 78 mg, 0.312 mmol). The reaction mixture was stirred for 18 hrs and evaporated under reduced pressure to remove the acetonitrile. The residue was dissolved in DCM and washed with water. The organic solution was dried over MgSO4 and evaporated under reduced pressure to afford the crude product which was purified by MDAP the title compound (39 mg) as a pale solid;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08377941B2
Source datasetuspto-grants-2013_02
ORD IDord-4ac2fe814afa4d03ad34ae06317e8c92
Source noteuspto-grants-2013_02