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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 874621Generated: October 30, 2026

Acetonitrile → HCID 58487345, compound

https://huagongshe.com/reaction/874621

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantHCID 58487036HCID 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 numberUS08980629B2
Source datasetuspto-grants-2015_03
ORD IDord-1148613647814d8ab29af9871237aab6
Source noteuspto-grants-2015_03