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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 889331Generated: October 26, 2026

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

https://huagongshe.com/reaction/889331

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, l8 mmol). LCMS: retention time 2.77 min MH30 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 numberUS08252818B2
Source datasetuspto-grants-2012_08
ORD IDord-bd3ea754627e4ba0a8ac983069e8c478
Source noteuspto-grants-2012_08