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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2106200Generated: October 31, 2026

Benzylamine → 1-Benzyl-3-(5-methyl-thiophen-2-yl)-4,5,6,7-tetrahydro-1H-pyrrolo[3,2-c]pyridine

https://huagongshe.com/reaction/2106200

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
Reactant2-Methyl-5-(2-nitro-vinyl)-thiopheneHCID 53915876—
Reactant1-Benzyl-3-(5-methyl-thiophen-2-yl)-1,4,6,7-tetrahydro-pyrrolo[3,2-c]pyridine-5-carboxylic acid tert-butyl esterHCID 67269441—
SolventTolueneHCID 1140—
Product1-Benzyl-3-(5-methyl-thiophen-2-yl)-4,5,6,7-tetrahydro-1H-pyrrolo[3,2-c]pyridineHCID 59752660—

Reaction Steps

1-Benzyl-3-(5-methyl-thiophen-2-yl)-1,4,6,7-tetrahydro-pyrrolo[3,2-c]pyridine-5-carboxylic acid tert-butyl ester. A mixture of 4-oxo-piperidine-1-carboxylic acid tert-butyl ester (0.54 g) and 300 μL of benzylamine in toluene (10 mL) was heated at reflux for 6 h using a Dean-Stark apparatus. The solution was cooled to RT and 0.47 g of 2-methyl-5-(2-nitro-vinyl)-thiophene was added. The mixture was stirred for 16 h at RT and then was concentrated in vacuo. The residue was chromatographed on SiO2 (1 to 30% EtOAc/hexanes) to afford 281.9 mg of the desired compound. TLC (SiO2, 33% EtOAc/hexanes): Rf=0.54

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07579470B2
Source datasetuspto-grants-2009_08
ORD IDord-ee28a0784062405b89a0d0b22f49d4b3
Source noteuspto-grants-2009_08