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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2365518Generated: October 31, 2026

4-Methylmorpholine → HCID 178508754, compound

https://huagongshe.com/reaction/2365518

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
Reactant3-(4-Benzyloxyphenyl)propionic acidHCID 561372—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 178508756HCID 178508756—
SolventDimethylformamideHCID 6228—
ProductHCID 178508754HCID 178508754—

Reaction Steps

(E)-3,5-diamino-6-chloro-N-(8-azaspiro[bicyclo[3.2.1]octane-3,4′-imidazolidine]-2′-ylidene)pyrazine-2-carboxamide (prepared as described for Ex. 252) (280 mg, 0.798 mmol) is dissolved in DMF (8 ml) along with HATU (303 mg, 0.798 mmol) and 3-(4-benzyloxy-phenyl)-propionic acid (205 mg, 0.798 mmol). N-Methyl morpholine (0.263 ml, 2.394 mmol) is added and the solution stirred at room temperature for 6 hours. The mixture is then concentrated in vacuo. EtOAc (100 ml) is added and the solution washed with water (100 ml). The organic phase is dried (MgSO4) and concentrated. The residue is dissolved in MeOH (20 ml) and dry loaded onto silica (5 g). Purification by flash chromatography (SiO2, DCM/MeOH) gives the title compound as a tan solid; [M+H]+ 589.20, 591.19 for Cl isotopes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697687B2
Source datasetuspto-grants-2014_04
ORD IDord-f4dee5a5349344c1969aa8df3b4238ff
Source noteuspto-grants-2014_04