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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2047404Generated: October 30, 2026

Piperidine → HCID 68672115, compound

https://huagongshe.com/reaction/2047404

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantTriethylamineHCID 8471—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 68670890HCID 68670890—
CatalystZincchlorideHCID 3007855—
SolventMethanolHCID 887—
ProductHCID 68672115HCID 68672115—

Reaction Steps

1-[3-(1-methyl-1H-benzo[d]imidazol-2-yl)phenyl]piperidin-4-one (0.06 g, 0.2 mmol) and piperidine (0.034 g, 0.4 mmol) with triethylamine (27 μL, 0.2 mmol) and molecular sieves (0.5 g) were heated to 40° C. in methanol (5 ml) for 16 hours. Sodiumcyanoborohydride (0.025 g, 0.4 mmol) and zinc chloride (0.027 g, 0.2 mmol) were added and the reaction heated for a further 16 hours, the reaction mixture was evaporated and the residue partitioned between 1N sodium hydroxide (2 ml) and dichloromethane (4 ml). The organic layer was separated, evaporated and purified by preparative HPLC.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592463B2
Source datasetuspto-grants-2013_11
ORD IDord-3389a78a905749df893614f880a67df6
Source noteuspto-grants-2013_11