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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1401400Generated: October 31, 2026

4-Methylphenylhydrazine monohydrochloride → 2-ethyl-8-methyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole

https://huagongshe.com/reaction/1401400

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methylphenylhydrazine monohydrochlorideHCID 12504—
Reactant1-Ethylpiperidin-4-one--hydrogen chloride (1/1)HCID 12319915—
SolventEthanolHCID 702—
Product2-ethyl-8-methyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indoleHCID 5945506691.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of p-tolylhydrazine hydrochloride (5.0 g, 31.5 mmol) in Ethanol (150 mL) was added 1-ethylpiperidin-4-one hydrochloride (4.0 g, 24.5 mmol) and heated at 80° C. for 16 h. After completion of the reaction (monitored by LCMS). The reaction mixture was concentrated to dryness and basified with aq. saturated NaHCO3, extracted with EtOAc, the organic layer was separated dried over sodium sulfate and concentrated under vacuum to obtain 4.8 g (Yield 71.0%) of 2-ethyl-8-methyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole. 1H NMR (CDCl3, free base) δ (ppm) 7.7 (bs, 1H), 7.2-7.1 (m, 2H), 6.9 (d, 1H), 3.8 (s, 2H), 2.9 (s, 4H), 2.7 (q, 2H), 2.4 (s, 3H), 1.2 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08907097B2
Source datasetuspto-grants-2014_12
ORD IDord-29c54278b6cf4357a7db2fe630950306
Source noteuspto-grants-2014_12