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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 225443Generated: October 25, 2026

Cesium carbonate → 5-(5-Amino-pyrazin-2-yl)-2-(2,6-dimethyl-morpholin-4-yl)-3,4-difluoro-benzaldehyde

https://huagongshe.com/reaction/225443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant2-Amino-5-bromopyrazineHCID 599539—
Reactanttoluene IPA waterHCID 66631872—
Reactant2-(2,6-Dimethyl-morpholin-4-yl)-3,4-difluoro-5-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-benzaldehydeHCID 76045223—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product5-(5-Amino-pyrazin-2-yl)-2-(2,6-dimethyl-morpholin-4-yl)-3,4-difluoro-benzaldehydeHCID 8661450135.9%

Reaction Conditions

Temperature85 °C

Reaction Steps

To a suspension of 2-(2,6-Dimethyl-morpholin-4-yl)-3,4-difluoro-5-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-benzaldehyde (0.500 g, 1.3 mmol) and cesium carbonate (1.2 g, 3.6 mmol) in previously degassed toluene/IPA/water (4/4/1) mixture (2.5 mL) was added 5-bromo-pyrazin-2-ylamine (Maybridge, 0.208 g, 1.2 mmol) under nitrogen. Tetrakis(triphenylphosphine)palladium-(0) (0.055 g, 0.05 mmol) was added at room temperature and the reaction was heated at 85° C. for 3.5 hrs. The mixture was cooled to room temperature, diluted with EtOAc and water then neutralized. The phases were separated and the aqueous phase was re-extracted with EtOAc (×2). The combined organic layers were dried over MgSO4 and concentrated. Purified by column chromatography eluting with ethyl acetate in hexanes (10-60%) to obtain 150 mgs of product. 1H NMR (400 MHz, CHLOROFORM-d) d ppm 1.28 (d, J=6.4 Hz, 6H), 2.97 (m, 2H), 3.34 (m, 2H), 4.18 (m, 2H), 4.78 (s, 2H), 8.08 (d, J=1.6 Hz, 1H), 8.19 (dd, J=8.4, 2.1 Hz, 1H), 8.44 (m, 1H), 10.37 (s, 1H); MS(APCl+) m/z 349 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557100B2
Source datasetuspto-grants-2009_07
ORD IDord-d1399685032946078dbe748a4f467f04
Source noteuspto-grants-2009_07