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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 630813Generated: October 29, 2026

Ammonia → 1-(6-Fluoro-[1,2,4]triazolo[4,3-a]pyridin-3-yl)-4-methyl-piperidin-4-ol

https://huagongshe.com/reaction/630813

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant4-Methylpiperidin-4-olHCID 15649174—
Reactant3-Chloro-6-fluoro-[1,2,4]triazolo[4,3-a]pyridineHCID 55267540—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product1-(6-Fluoro-[1,2,4]triazolo[4,3-a]pyridin-3-yl)-4-methyl-piperidin-4-olHCID 8668709732.7%

Reaction Conditions

Temperature170 °C

Reaction Steps

A mixture of Intermediate 24b (400 mg, 2.32 mmol) and Intermediate 79b (1.33 g, 11.6 mmol) in NMP (5 mL) was heated in the microwave at 170° C. for 3 h. The reaction mixture was applied to an SCX-2 cartridge (25 g) and washed with MeOH. The product was eluted with 2M NH3 in MeOH; concentration in vacuo gave a residue. FCC, using 0-8% [2M NH3 in MeOH] in DCM, gave the title compound (190 mg, 32%). LCMS (Method 1): Rt 2.01 min, m/z 251 [MH+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315503B2
Source datasetuspto-grants-2016_04
ORD IDord-66c888fa5b0f4950b66af9be9170e32b
Source noteuspto-grants-2016_04