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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2070892Generated: October 31, 2026

4-Methylmorpholine → HCID 68587925, compound

https://huagongshe.com/reaction/2070892

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
Reactant4-Amino-1-Boc-piperidineHCID 1268291—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 68587964HCID 68587964—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 68587925HCID 6858792572%

Reaction Steps

tert-Butyl 4-(4-(5-phenyl-[1,2,4]triazolo[1,5-a]pyridin-2-ylamino)benzamido) piperidine-1-carboxylate. A mixture of 4-(5-phenyl-[1,2,4]triazolo[1,5-a]pyridin-2-ylamino)benzoic acid (200 mg, 0.6 mmol), tert-butyl 4-aminopiperidine-1-carboxylate (121 mg, 0.6 mmol), 2-(3H-[1,2,3]triazolo[4,5-b]pyridin-3-yl)-1,1,3,3-tetramethylisouronium hexafluorophosphate(V) (460 mg, 1.2 mmol) and N-methylmorpholine (306 mg, 3.0 mmol) in N,N-dimethylformamide (2 mL) was stirred at room temperature overnight. Water (5 mL) was added, and the precipitate was collected by filtration and washed with water to give tert-butyl 4-(4-(5-phenyl-[1,2,4]triazolo[1,5-a]pyridin-2-ylamino)benzamido)piperidine-1-carboxylate (220 mg, 72% yield) as a solid. MS (ESI): m/z 535.1 [M+23]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299056B2
Source datasetuspto-grants-2012_10
ORD IDord-4c543e8b13a346c09c5a05918ddf33de
Source noteuspto-grants-2012_10