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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2173713Generated: October 29, 2026

4-Methylmorpholine → HCID 178508421, compound

https://huagongshe.com/reaction/2173713

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—
ReactantHCID 58442296HCID 58442296—
ReactantHCID 178507695HCID 178507695—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 178508421HCID 178508421—

Reaction Steps

A mixture, comprising 3-amino-6-bromo-5-trifluoromethyl-pyrazine-2-carboxylic acid (Intermediate 2)(0.349 g, 1.221 mmol), 3-(piperidin-1-ylmethyl)-1H-pyrazol-5-amine (Intermediate 8) (0.220 g, 1.221 mmol), HATU (0.464 g, 1.221 mmol) and N-methylmorpholine (0.241 ml, 2.441 mmol) in DMF (5 ml) was stirred for 30 minutes at RT. The reaction mixture was diluted with water (20 ml) and the resulting yellow precipitate was filtered under vacuum and washed with water (20 ml). The resulting residue was loaded onto a SCX-2 cartridge eluting with MeOH followed by 7M NH3 in MeOH. The methanolic ammonia fractions were concentrated in vacuo and the residue was triturated with EtOAc/iso-hexane to yield the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056867B2
Source datasetuspto-grants-2015_06
ORD IDord-1ccc1d91666f48ed8158f52af3d6f8de
Source noteuspto-grants-2015_06