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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2173717Generated: November 1, 2026

4-Methylmorpholine → HCID 71533330, compound

https://huagongshe.com/reaction/2173717

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
Reactant4-(2-Pyridinyl)-1H-pyrazol-3-amineHCID 1477762—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant3-Amino-6-bromo-5-trifluoromethyl-pyrazine-2-carboxylic acidHCID 58442296—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 71533330HCID 71533330—

Reaction Steps

A mixture comprising 3-amino-6-bromo-5-trifluoromethyl-pyrazine-2-carboxylic acid (Intermediate 2) (0.179 g, 0.624 mmol), 5-amino-4-(pyridin-2-yl)-1H-pyrazole (0.1 g, 0.624 mmol), HATU (0.237 g, 0.624 mmol) and N-methylmorpholine (0.123 ml, 1.249 mmol) in DMF (5 ml) was stirred at 80° C. for 2.5 hours. After cooling to RT, the mixture was diluted with water (40 ml) and the resulting yellow precipitate was filtered under vacuum and washed with water (20 ml). MeOH (150 ml) was added to the solid and the suspension ultrasonicated to give a fine suspension. The suspension was filtered under vacuum and the solid was rinsed with MeOH (20 ml) and dried under vacuum at 45° C. for 1.5 hours to afford the title compound as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056867B2
Source datasetuspto-grants-2015_06
ORD IDord-e5e86b7a72c84dabb34c2e4825ddab7e
Source noteuspto-grants-2015_06