Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2382768Generated: November 2, 2026

Cyclohexanol → HCID 25216188, compound

https://huagongshe.com/reaction/2382768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanolHCID 7966—
ReactantSodium hydrideHCID 24758—
Reactant5-Chloro-[1,2,4]triazolo[1,5-a]pyridin-2-amineHCID 21464413—
SolventTetrahydrofuranHCID 8028—
ProductHCID 25216188HCID 2521618880.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

Cyclohexanol (1.68 mL; 15.84 mmol; 5.0 eq.) was added to a suspension of NaH (152 mg; 3.80 mmol; 1.2 eq.) in THF (6.0 mL) and maintained under inert atmosphere at 0° C. The reaction mixture was brought back to rt and stirred for 1 h before the addition of 5-chloro[1,2,4]triazolo[1,5-a]pyridin-2-amine ((A4), 534 mg; 3.17 mmol; 1.0 eq.). Reaction mixture was then heated at reflux for 3 h after which time it was quenched by addition of water. It was then extracted with EtOAc, washed with brine, dried over magnesium sulfate, filtered and concentrated. Purification by flash chromatography on silica gel (DCM/MeOH, 95:5 to 10:90) gave the title compound as a white solid (590 mg, 80%). HPLC, Rt: 2.18 min. (purity 90.1%). LC/MS, M+(ESI): 233.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263595B2
Source datasetuspto-grants-2012_09
ORD IDord-c19b3b8b4d064619a9c67c3db3309a1f
Source noteuspto-grants-2012_09