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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716501Generated: November 1, 2026

2-Amino-4-methylpyridine → HCID 44178123, compound

https://huagongshe.com/reaction/1716501

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-4-methylpyridineHCID 1533—
ReactantCesium carbonateHCID 10796—
ReactantBinap, (A+-)-HCID 634876—
ReactantHCID 58706639HCID 58706639—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 44178123HCID 4417812338.2%

Reaction Conditions

Temperature100 °C

Reaction Steps

4-[5-(6-bromopyridin-2-yl)thiazol-2-yl]-1-methylpiperazin-2-one obtained in Step 5 (188 mg, 0.53 mmol) was dissolved in toluene (5 ml), and after 2-amino-4-methylpyridine (58 mg, 0.53 mmol) was added, 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (66 mg, 0.11 mmol), palladium acetate (18 mg, 0.08 mmol) and cesium carbonate (260 mg, 0.80 mmol) were added and the mixture was stirred overnight at 100° C. Water was added to the reaction solution and extracted with ethyl acetate and the organic layer was washed with a saturated saline solution. The organic layer was dried over sodium sulfate and after vacuum concentration, the residue was washed with methanol and the title compound (77 mg, 38%) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803801B2
Source datasetuspto-grants-2010_09
ORD IDord-1a3a0c687a38470db48c8c096f4b6e71
Source noteuspto-grants-2010_09