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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428918Generated: November 1, 2026

4-Methylmorpholine → HCID 53379822, compound

https://huagongshe.com/reaction/1428918

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantN-methylpyridazin-4-amineHCID 23080684—
ReactantHCID 62054042HCID 62054042—
SolventDimethylformamideHCID 6228—
ProductHCID 53379822HCID 5337982267%

Reaction Steps

O-(7-Azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphat (HATU; 1.23 g, 3.24 mmol, 3.00 eq) and N-methylmorpholine (0.71 ml, 0.66 g, 6.5 mmol, 6.0 eq) was added to a solution of 1-(2-methoxyethyl)-5-methyltriazole-4-carboxylic acid (200 mg, 1.08 mmol) and N-methylpyridazin-4-amine (118 mg, 1.08 mmol, 1.00 eq) in DMF (2.5 ml) and the mixture was stirred at room temperature for 4 d. After removal of the solvent, the residue was dissolved in dichloromethane, washed twice with sat. aq. NaHCO3 sol. and once with brine and dried over Na2SO4. Removal of the solvent under vacuum and chromatographic purification (CH:EtOAc) gave the title compound as a brown oil (200 mg, 64%, 95% purity).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08937177B2
Source datasetuspto-grants-2015_01
ORD IDord-6a2dc1d44a664c058abd62ba700e2ac4
Source noteuspto-grants-2015_01