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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 62507Generated: October 30, 2026

Cesium carbonate → HCID 46215100, compound

https://huagongshe.com/reaction/62507

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantBinap, (A+-)-HCID 634876—
Reactant1-Isobutyl-4-methyl-1H-pyrazol-5-amineHCID 21455612—
Reactant2-[(2,5-dichloro-4-pyridinyl)amino]-N-(methyloxy)benzamideHCID 57516896—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
ProductHCID 46215100HCID 46215100—

Reaction Conditions

Temperature90 °C

Reaction Steps

A microwave tube was charged with 2-[(2,5-dichloro-4-pyridinyl)amino]-N-(methyloxy)benzamide (300 mg, 0.96 mmol), 4-methyl-1-(2-methylpropyl)-1H-pyrazol-5-amine (309 mg, 2.01 mmol), cesium carbonate (939 mg, 2.88 mmol) and DMF (5 ml). The reaction mixture was degassed under nitrogen for 10 min, and palladium (II) acetate (10.8 mg, 0.05 mmol) and BINAP (59.8 mg, 0.096 mmol) were added. The reaction mixture was heated in an oil bath at 90° C. for 5 hrs and then in a microwave at 150° C. for 40 min. Solvent was evaporated and the residue was dissolved in MeOH, filtered thru celite and thru an Acrodisc an purified further using preparative Agilent HPLC (5 to 95% water:acetonitrile with 0.1% formic acid). Fractions were combined and evaporated. The brown oil residue was diluted in DMF and water was added. A precipitate crashed out. It was filtered off and dried under vacuum at 40° C. for 5 hrs. LC-MS [M+H]+=429.1. 1H NMR (400 MHz, DMSO-d6) ppm 11.93 (s, 1 H) 9.48 (br. s., 1 H) 8.26 (s, 1 H) 7.94 (s, 1 H) 7.58 (d, J=7.33 Hz, 1 H) 7.44-7.51 (m, 2 H) 7.23 (s, 1 H) 7.08-7.16 (m, 1 H) 6.38 (s, 1 H) 3.70 (s, 3 H) 3.65 (d, J=7.33 Hz, 2 H) 2.03 (dt, J=13.71, 6.92 Hz, 1 H) 1.77 (s, 3 H) 0.75 (d, J=6.57 Hz, 6 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09446034B2
Source datasetuspto-grants-2016_09
ORD IDord-3a064487f80a4173a08fb870f69034f9
Source noteuspto-grants-2016_09