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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2381938Generated: October 30, 2026

Water → 2-(Pyridin-2-yl)pyrimidine-5-carboxylic acid-(4-fluoroindol-1-yl)amide

https://huagongshe.com/reaction/2381938

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 68553171HCID 68553171—
ReactantHCID 86639367HCID 86639367—
SolventEthyl AcetateHCID 8857—
Product2-(Pyridin-2-yl)pyrimidine-5-carboxylic acid-(4-fluoroindol-1-yl)amideHCID 2509965817.3%

Reaction Steps

A suspension of 2-(pyridine-2-yl)-pyrimidine-5-carbonyl chloride (0.44 g) in EtOAc (20 mL) is added portion wise to a mixture of 1-amino-4-fluoroindole (0.30 g) and K2CO3 (0.276 g) in EtOAc (10 mL)/water (20 mL) and the resulting mixture is stirred at rt for 24 h. The aqueous phase is separated and extracted twice with EtOAc. The combined organic layer is washed with water and brine, dried (MgSO4), filtered and concentration in vacuo. The residue is purified by silica gel chromatography eluting with EtOAc to afford 2-(pyridin-2-yl)pyrimidine-5-carboxylic acid-(4-fluoroindol-1-yl)amide (0.115 g, 17%) as a solid. MS: 334 (M+H); 1H NMR (300 MHz, DMSO-d6): δ 6.65 (d, 1H), 6.89-6.95 (q, 1H), 7.16-7.23 (m, 1H), 7.32-7.35 (d, 1H), 7.57 (d, 1H), 7.57-7.64 (m, 1H), 8.02-8.08 (t, 1H), 8.50-8.52 (d, 1H), 8.82-8.83 (d, 1H), 9.49 (s, 2H), 12.30 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258130B2
Source datasetuspto-grants-2012_09
ORD IDord-c687b198df5143e996952f0e5c03122c
Source noteuspto-grants-2012_09