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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1262582Generated: November 2, 2026

1-Aminopyrrole → HCID 20263906, compound

https://huagongshe.com/reaction/1262582

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 numberUS04452803
Source datasetuspto-grants-1984_06
ORD IDord-409e62bd6453487799840a07acd9695a
Source noteuspto-grants-1984_06