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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 749723Generated: October 25, 2026

tert-Butyl 4-oxopiperidine-1-carboxylate → 1-Benzyl-3-(3-chloro-phenyl)-4,5,6,7-tetrahydro-1H-pyrrolo[3,2-c]pyridine

https://huagongshe.com/reaction/749723

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
Reactant1-Chloro-3-(2-nitroethenyl)benzeneHCID 2731646—
SolventBenzylamineHCID 7504—
Product1-Benzyl-3-(3-chloro-phenyl)-4,5,6,7-tetrahydro-1H-pyrrolo[3,2-c]pyridineHCID 5331660948.9%

Reaction Steps

The title compound (193.3 mg) was prepared from 0.50 g of 4-oxo-piperidine-1-carboxylic acid tert-butyl ester, 260 μL of benzylamine, and 0.45 g of 1-chloro-3-(2-nitro-vinyl)-benzene as in Example 9. MS (ESI): exact mass calculated for C20H19ClN2, 322.12; found, m/z 323.2 [M+H]+. 1H NMR (500 MHz, CDCl3): 7.36-7.20 (m, 6H), 7.14-7.07 (m, 3H), 6.81 (s, 1H), 5.01 (s, 2H), 4.04 (s, 2H), 3.14 (t, J=5.8 Hz, 2H), 2.51 (t, J=5.8 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07402680B2
Source datasetuspto-grants-2008_07
ORD IDord-8a3bee805f984adb92f6cce27505fd11
Source noteuspto-grants-2008_07