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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2382883Generated: October 30, 2026

Pyridine → HCID 59437496, compound

https://huagongshe.com/reaction/2382883

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantMorpholineHCID 8083—
ReactantN5-cyclohexyl[1,2,4]triazolo[1,5-a]pyridine-2,5-diamineHCID 25216186—
ReactantHCID 86643869HCID 86643869—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59437496HCID 594374969.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

Pyridine (198 mg; 2.5 mmol; 5.0 eq.) was added to a solution of N5-cyclohexyl[1,2,4]triazolo[1,5-a]pyridine-2,5-diamine ((A9), 116 mg; 0.50 mmol; 1.0 eq.) in DCM (2.0 mL). 6-(chloromethyl)pyridine-3-carbonyl chloride hydrochloride (190 mg; 1.0 mmol; 2.0 eq.) was added and the resulting black solution was stirred under reflux for 14 h. The solvents were evaporated to yield a black oil. Morpholine (218 mg; 2.5 mmol; 5.0 eq.) and THF (0.5 mL) were added to this residue, and the mixture was then stirred and heated at 60° C. for 12 h. Purification by RP-HPLC (Waters Sunfire™ Prep C18 OBD™ 5 μM, 100×49 mm) following a gradient starting with 20/80 (0.1% formic acid in CH3CN/0.1% formic acid in H2O) up to 95/5 in 12 min. The fractions were collected and lyophilized to give the title compound as a white powder (20 mg, 9%). HPLC, Rt: 2.11 min. (purity 100%). LC/MS, M+(ESI): 436.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263595B2
Source datasetuspto-grants-2012_09
ORD IDord-17c9a930b34843bdac828600c9566a35
Source noteuspto-grants-2012_09