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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464048Generated: October 29, 2026

1-Aminopyrrole → HCID 20263906, compound

https://huagongshe.com/reaction/464048

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-AminopyrroleHCID 136589—
ReactantSodium borohydrideHCID 4311764—
Reactant4-Piperidinone, 1-[2-(2-thienyl)ethyl]-HCID 11052887—
SolventBenzeneHCID 241—
ProductHCID 20263906HCID 20263906—

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of 1-(2-thienylethyl)-4-piperidone (24.6 g, 0.12 mole) and 1-aminopyrrole (12 g, 0.15 mole) in 200 ml of benzene was stirred at reflux for 4 hours. The resultant mixture was cooled and evaporated to an oil which in turn was dissolved in 200 ml of isopropanol and 50 ml of methanol. To the resultant solution was added NaBH4 (9.1 g, 0.24 mole). The mixture was stirred at 80° C. for 2 hours, cooled, evaporated, stirred with water and then extracted with ethyl acetate-ether. The organic extract was washed twice with water and saturated NaCl solution and was dried (anhydrous MgSO4), filtered and evaporated to 33 g of an oil of 1-[2-(2-thienyl)ethyl]-4-(1H-pyrrol-1-yl)aminopiperidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04546105
Source datasetuspto-grants-1985_10
ORD IDord-765d9eb881c2454f9a152d29f614bcd4
Source noteuspto-grants-1985_10