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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 630724Generated: October 31, 2026

Ammonia → HCID 86686988, compound

https://huagongshe.com/reaction/630724

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantPiperidin-4-olHCID 79341—
Reactant3-Chloro-6-fluoro-[1,2,4]triazolo[4,3-a]pyridineHCID 55267540—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
SolventDimethylacetamideHCID 31374—
ProductHCID 86686988HCID 8668698844%

Reaction Steps

A brown solution of Intermediate 24b (855 mg, 4.98 mmol) and 4-hydroxypiperidine (2.02 g, 19.9 mmol) in DMA (15 mL) was irradiated to 175° C. in the microwave for 3 h. The cooled solution was concentrated in vacuo, then the residue diluted with water (20 mL) and brine (20 mL). The mixture was washed with diethyl ether (2×50 mL), then extracted with EtOAc (2×50 mL). The combined EtOAc layers were washed with brine (50 mL), dried (Na2SO4), filtered and concentrated in vacuo to leave a yellow oil. The aqueous was further extracted with DCM (3×50 mL). The combined DCM layers were passed through a hydrophobic frit and concentrated in vacuo to leave a brown oil. The two oils were combined. FCC, using 4-5% [2M NH3 in MeOH] in DCM, gave the title compound as a yellow crystalline solid (514 mg, 44%). LCMS (Method 3): Rt 1.96 min, m/z 237 [MH+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315503B2
Source datasetuspto-grants-2016_04
ORD IDord-f67acf3523774139a943be5c8a8e1105
Source noteuspto-grants-2016_04