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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 68553171 | HCID 68553171 | — |
| Reactant | HCID 86639367 | HCID 86639367 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-(Pyridin-2-yl)pyrimidine-5-carboxylic acid-(4-fluoroindol-1-yl)amide | HCID 25099658 | 17.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08258130B2 |
|---|
| Source dataset | uspto-grants-2012_09 |
|---|
| ORD ID | ord-c687b198df5143e996952f0e5c03122c |
|---|
| Source note | uspto-grants-2012_09 |
|---|