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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 728764Generated: October 27, 2026

Hydrochloric Acid → HCID 57016353, compound

https://huagongshe.com/reaction/728764

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-AzaindoleHCID 9226—
ReactantPiperidone monohydrate hydrochlorideHCID 22021827—
SolventMethanolHCID 887—
ProductHCID 57016353HCID 57016353—

Reaction Steps

To a stirred solution of Na (2.53 g, 110 mmol, 11 eq) in absolute methanol (50 ml) at room temperature was added the appropriate pyrrolopyridine (10.00 mmol) and piperidone monohydrate hydrochloride (4.60 g, 30.0 mmol, 3.0 eq). The resultant mixture was then heated at reflux under nitrogen for 2-24 hours depending on the substrate. The resultant reaction mixture was cooled, and concentrated hydrochloric acid (37%, 9.0 ml, 110 mmol) wasadded dropwise with vigorous stirring. The resultant mixture was then evaporated under reduced pressure, and the residual slurry placed in water(50 ml). This aqueous mixture was extracted with ethyl acetate (5×50 ml), and these extracts were combined, dried (Na2SO4), and evaporated under reduced pressure. The residue was either triturated directly or column chromatographed using silica gel (approximately 100 g) and elution with the appropriate solvent system yielding the desired 3-(1,2,5,6-tetrahydropyridyl)pyrrolopyridine, one of Compounds 1a-1m or compound 2, 3a, 3b, 3c or 4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05051412
Source datasetuspto-grants-1991_09
ORD IDord-ae26a406a338428795051bd3c4acfd14
Source noteuspto-grants-1991_09