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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2106757Generated: October 31, 2026

Ethyl piperidine-2-carboxylate → HCID 15125474, compound

https://huagongshe.com/reaction/2106757

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl piperidine-2-carboxylateHCID 27517—
Reactant1,4-DioxaneHCID 31275—
ReactantPhenyl N-(4-(4-(4-methoxyphenyl)piperazin-1-yl)phenyl)carbamateHCID 981607—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventWaterHCID 962—
ProductHCID 15125474HCID 1512547447.5%

Reaction Steps

A mixture of 50 parts of phenyl [4-[4-(4-methoxyphenyl)-1-piperazinyl]phenyl]carbamate, 22.7 parts of ethyl 2-piperidinecarboxylate, 4 parts of N,N-dimethyl-4-pyridinamine and 300 parts of 1,4-dioxane was stirred for 5 hours at reflux temperature. After saturation with water, the reaction mixture was heated for 30 minutes. After cooling, the precipitated product was filtered off, washed with 2-propanol and purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (99:1 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from 1-butanol. The product was filtered off and dried, yielding 24.8 parts (47.5%) of 5,6,7,8-tetrahydro-2-[4-[4-(4-methoxyphenyl)-1-piperazinyl]phenyl]imidazo[1,5-a]pyridine-1,3(2H,8aH)-dione; mp. 223.4° C. (int. 17).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04931444
Source datasetuspto-grants-1990_06
ORD IDord-f14e97475c584bc6bc2c61d7a54933be
Source noteuspto-grants-1990_06