Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397550Generated: October 25, 2026

2-Bromopropane → 1-Isopropylpyridinium-4-carboxamide bromide

https://huagongshe.com/reaction/397550

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopropaneHCID 6358—
ReactantIsonicotinamideHCID 15074—
SolventDimethylformamideHCID 6228—
Product1-Isopropylpyridinium-4-carboxamide bromideHCID 2349776165%

Reaction Steps

A solution of 200 mL of DMF, containing 50.0 g of isonicotinamide and 60 mL of 2-bromopropane, was refluxed 5.75 h. A white insoluble solid filtered from this cool solution gave 64.9 g (65%) of 1-isopropylpyridinium-4-carboxamide bromide, m/e=165, NMR. Catalytic reduction of this salt, with PtO2 in MeOH, gave 65.2 g (98%) of 1-isopropylpiperidine-4-carboxamide hydrobromide, m/e=171. An aqueous solution of this salt was basified, evaporated to dryness, and extracted with EtOAc to give 39.7 g (90%) of 1-isopropylpiperidine-4-carboxamide free base.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610704B1
Source datasetuspto-grants-2003_08
ORD IDord-2b9dddca4f9940ed9ffd353189dd5876
Source noteuspto-grants-2003_08