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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 524949Generated: October 28, 2026

Methanol → HCID 86721005, compound

https://huagongshe.com/reaction/524949

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant3-OxetanoneHCID 15024254—
ReactantHCID 86721004HCID 86721004—
Reactant1H-benzo[d][1,2,3]triazol-1-yl 2-amino-6-(cyanomethyl)pyrazolo[1,5-a]pyrimidine-3-carboxylateHCID 90199892—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86721005HCID 8672100592.3%

Reaction Steps

Sodium triacetoxyborohydride (Sodium Ion (1)) (1.189 g, 5.608 mmol) was added in portions to a stirred solution of 3-nitro-4-(1,2,3,6-tetrahydropyridin-4-yl)pyridine (523 mg, 2.549 mmol) and 3-oxetanone (312.2 mg, 277.8 μL, 4.333 mmol) in THF (10 mL) at 0° C. under an atmosphere of nitrogen. The reaction was allowed to warm to ambient temperature and was stirred for 16 hours. MeOH (2 mL) was added dropwise and the mixture stirred at ambient temperature for 30 minutes. The mixture was concentrated in vacuo and the residue was partitioned between water and EtAOc. The pH of the aqueous layer was adjusted to pH 7-8 by the addition of NH4OH and the layers separated. The aqueous layer was extracted with EtOAc (×3) and the combined organic extracts washed with brine (×1), dried (MgSO4), filtered and concentrated in vacuo to give 3′-nitro-1-(oxetan-3-yl)-1,2,3,6-tetrahydro-4,4′-bipyridine as a red oil (615 mg, 92% Yield). MS (ES+) 262.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09340546B2
Source datasetuspto-grants-2016_05
ORD IDord-4a6a7fd7b4f74ccca34ba7a12020d13e
Source noteuspto-grants-2016_05