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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2112973Generated: October 30, 2026

Cyclohexylamine → HCID 86235182, compound

https://huagongshe.com/reaction/2112973

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexylamineHCID 7965—
ReactantHCID 57643138HCID 57643138—
ProductHCID 86235182HCID 86235182—

Reaction Steps

A mixture of cyclohexylamine (4 mL) and 5-chloro-7-pyridin-3-yl-[1,2,4]triazolo[1,5-a]pyridin-2-ylamine, which may be produced as in Example 1A, (280 mg, 1.14 mmol) was microwaved at 155° C. for 1 h. On cooling, the product was triturated with toluene/cyclohexane, then taken up in CH2Cl2 and washed with aqueous Na2CO3. The organic layer was separated, dried (MgSO4), then concentrated to provide N5-cyclohexyl-7-(pyridin-3-yl)-[1,2,4]triazolo[1,5-a]pyridine-2,5-diamine. MS m/z 309 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07524860B2
Source datasetuspto-grants-2009_04
ORD IDord-b806102430c64ff9a4d9790d5c27a5d9
Source noteuspto-grants-2009_04