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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108958Generated: November 2, 2026

Pyrrolidine → N-(3-iodo-4-methylphenyl)-2-pyrrolidin-1-yl-isonicotinamide

https://huagongshe.com/reaction/2108958

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrrolidineHCID 31268—
Reactant2-Chloro-N-(3-iodo-4-methylphenyl)pyridine-4-carboxamideHCID 21914557—
ProductN-(3-iodo-4-methylphenyl)-2-pyrrolidin-1-yl-isonicotinamideHCID 21914627—

Reaction Steps

A solution of N-(3-iodo-4-methylphenyl)-2-chloro-isonicotinamide (Intermediate 20) (7.00 g, 18.8 mmol) in pyrrolidine (20 ml) was heated at 80° C. under an atmosphere of nitrogen for 16 hours. Excess pyrrolidine was removed in vacuo and the residue was titurated with dietheyl ether (20 ml). The resulting solid was collected by filtration and dried in vacuo to give N-(3-iodo-4-methylphenyl)-2-pyrrolidin-1-yl-isonicotinamide as a pale yellow solid (7.73 g, 18 mmol). LCMS: retention time 2.77 min MH+408. NMR: δH [2H6]-DMSO 10.29 (1H, s), 8.29 (1H, d), 8.20 (1H, d), 7.71 (1H, dd), 7.72 (1H, dd), 6.97 (1H, brd), 6.88 (1H, b), 3.45 (2H, apparent t), 3.09 (2H, m), 2.35 (3H, s), 1.98 (2H, m), 1.82 (2H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07514456B2
Source datasetuspto-grants-2009_04
ORD IDord-47d414de81924327849ede439bd1f87a
Source noteuspto-grants-2009_04