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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1036094Generated: November 1, 2026

Acetonitrile → HCID 58487345, compound

https://huagongshe.com/reaction/1036094

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantN-(6-amino-5-bromo(2-pyridyl))(2-fluorophenyl)carboxamideHCID 58487036—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 58487345HCID 584873454%

Reaction Conditions

Temperature85 °C

Reaction Steps

A mixture of N-(6-amino-5-bromo(2-pyridyl))(2-fluorophenyl)carboxamide (61) (16 mg, 0.05 mmol), bis(ditertbutyl(4-dimethylaminophenyl)phosphine)dichloropalladium (II) (4 mg, 10% mol) and K3PO4 (11 mg, 0.05 mmol) in 0.5 ml ACN, 0.5 ml dioxane, 0.2 ml H2O was bubbled with argon before heated at 85° C. for 4 h. After cooling down to r.t., the reaction mixture was taken up in EA, washed with aq. NaHCO3 and brine. Org. phase was dried over Na2SO4, concentrated to dryness. Flash silica gel column purification (0-90% B, A: hexane; B: 50% EA in hexane) furnished 2.2 mg crude desired product as yellow solid which was re-purified on prep HPLC to give 0.8 mg N-[6-amino-5-(1-methyl-3-phenylpyrazol-5-yl)(2-pyridyl)](2-fluorophenyl)carboxamide (69) as off-white solid. (yield: 4%, purity>90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546403B2
Source datasetuspto-grants-2013_10
ORD IDord-a60c8cf1b6154e6299389adaaa2e4e22
Source noteuspto-grants-2013_10