Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 60100Generated: October 29, 2026

Acetonitrile → HCID 53261783, compound

https://huagongshe.com/reaction/60100

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl IsocyanateHCID 12228—
ReactantN-(2,4-difluoro-3-[5-(1H-indazol-5-yl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl]-phenyl}-2,5-difluoro-benzenesulfonamideHCID 53261782—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 53261783HCID 5326178372.5%

Reaction Conditions

Temperature140 °C

Reaction Steps

Into a reaction flask, methyl isocyanate (6.5 mg, 0.11 mmol) is combined with N-{2,4-difluoro-3-[5-(1H-indazol-5-yl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl]-phenyl}-2,5-difluoro-benzenesulfonamide (P-0002, 22 mg, 0.031 mmol), tetrakis(triphenylphosphine)palladium(0) (2.2 mg, 0.0019 mmol), potassium carbonate (1.0 mL, 1.0 M in water) and 3 mL of acetonitrile. The reaction is heated at 140° C. for 50 minutes in a microwave, then diluted with water and ethyl acetate. The organic layer is washed with saturated sodium bicarbonate, then brine and dried over sodium sulfate, filtered and the filtrate concentrated under vacuum. The resulting material is purified by silica gel column chromatography, eluting with methanol and dichloromethane. Appropriate fractions are combined and concentrated under vacuum to provide the desired compound (P-0003, 14 mg, 72%). MS (ESI) [M+H+]+=623.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09440969B2
Source datasetuspto-grants-2016_09
ORD IDord-97c1aaf35b4b4ee3bf5e23f12f05c727
Source noteuspto-grants-2016_09