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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972150Generated: November 3, 2026

Potassium Phosphate, Tribasic → 3-(2-(4-(1-Acetylpiperidin-4-yl)thiazol-2-ylamino)pyridin-4-yloxy)isonicotinonitrile hydrochloride

https://huagongshe.com/reaction/1972150

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
Reactant3-(2-Chloropyridin-4-yloxy)isonicotinonitrileHCID 24994657—
Reactant1-(4-(2-Aminothiazol-4-yl)piperidin-1-yl)ethanoneHCID 59610036—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Product3-(2-(4-(1-Acetylpiperidin-4-yl)thiazol-2-ylamino)pyridin-4-yloxy)isonicotinonitrile hydrochlorideHCID 2486414012.71%

Reaction Conditions

Temperature90 °C

Reaction Steps

3-(2-Chloropyridin-4-yloxy)isonicotinonitrile (0.0650 g, 0.281 mmol) (prepared as in Example 2), 1-(4-(2-aminothiazol-4-yl)piperidin-1-yl)ethanone (0.0822 g, 0.365 mmol), potassium phosphate (0.137 g, 0.421 mmol), tris(dibenzylideneacetone)dipalladium (0) (0.00642 g, 0.00701 mmol) and 9,9-dimethyl-4,5-bis(diphenylphosphino)xanthene (0.00812 g, 0.0140 mmol) were combined and the vessel was capped with rubber septum. The vessel was evacuated and purged with nitrogen three times. Toluene (2 mL) and degassed water (2 mL) were added and the resulting mixture was heated to 90° C. and agitated overnight. After cooling the mixture was diluted with 50 ml of ethyl acetate and washed with sodium bicarbonate, brine, dried and evaporated. The crude product was purified by preparative HPLC (Parallex) and converted to HCl salt by treatment with 2M HCl in ether to provide the title compound (0.0150 g, 12.71% yield) as white solid. 1H NMR (CDCl3) δ 1.52-1.62 (m, 2H), 1.98-2.06 (m, 2H), 2.10 (s, 3H), 2.65 (t, 1H), 2.80 (t, 1H), 3.13 (t, 1H), 3.85(d, 1H), 4.66 (d, 1H), 6.35 (s, 1H), 6.45 (s, 1H), 6.50 (d, 1H), 7.15 (s, 1H), 7.40 (d, 1H), 8.05 (s, 1H), 9.01 (bs, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431713B2
Source datasetuspto-grants-2013_04
ORD IDord-bf0d8478606b4740be904a1bd26e21fb
Source noteuspto-grants-2013_04