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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1869624Generated: November 1, 2026

1,1-Dimethylethyl 4-[(1-cyclobutyl-4-piperidinyl)methyl]-1-piperidinecarboxylate → 1-Cyclobutyl-4-(4-piperidinylmethyl)piperidine

https://huagongshe.com/reaction/1869624

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1-Dimethylethyl 4-[(1-cyclobutyl-4-piperidinyl)methyl]-1-piperidinecarboxylateHCID 68886620—
Solvent1,4-Dioxane hydrochlorideHCID 20443148—
Product1-Cyclobutyl-4-(4-piperidinylmethyl)piperidineHCID 68886796—

Reaction Steps

1,1-Dimethylethyl 4-[(1-cyclobutyl-4-piperidinyl)methyl]-1-piperidinecarboxylate (may be prepared as described in Description 5) (5.7 g) was stirred in a solution of HCl-Dioxane (100 ml, 4M) for 1 h. The solvent was evaporated and the resultant yellow solid was dissolved in saturated potassium carbonate (25 ml). The solution was extracted into dichloromethane (3×50 ml) and the combined organics dried (MgSO4) and evaporated to give the title compound (D6) as a pale yellow oil which solidified on standing (3.04 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07638631B2
Source datasetuspto-grants-2009_12
ORD IDord-0209d218afad4217a0d6227676954daf
Source noteuspto-grants-2009_12