Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989199Generated: October 31, 2026

Sodium Carbonate → 1-(3-Fluoro5-(4-methyl-3-pyridyl)phenylcarbamoyl)-5-methoxy-6-trifluoromethylindoline

https://huagongshe.com/reaction/989199

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4-Methylpyridine-3-Boronic AcidHCID 2762711—
Reactant1-(3-Fluoro-5-iodophenylcarbamoyl)-5-methoxy-6-trifluoromethylindolineHCID 18005143—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Product1-(3-Fluoro5-(4-methyl-3-pyridyl)phenylcarbamoyl)-5-methoxy-6-trifluoromethylindolineHCID 18005152—

Reaction Steps

A mixture of 1-(3-fluoro-5-iodophenylcarbamoyl)-5-methoxy-6-trifluoromethylindoline (D17, 0.31 g, 0.65 mmol), 4-methyl-3-pyridylboronic acid (88 mg, 0.65 mmol), tetrakis (triphenylphosphine) palladium (0) (23 mg, 0.02 mmol) and sodium carbonate (0.31 g, 3.0 mmol) in 1,2-dimethoxyethane (20 mL) and water (2 mL) was heated under reflux for 24 h, then cooled and poured into water. The aqueous mixture was extracted with dichloromethane/methanol, and the organic extract was washed with brine, dried and evaporated. The residue was chromatographed on silica gel eluted with 2-3% methanol/dichloromethane to give the title compound, which was recrystallised from dichloromethane/petrol (80 mg, 28%), m.p. 191-5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06638953B2
Source datasetuspto-grants-2003_10
ORD IDord-173da943f4af4dc5b860054466aad257
Source noteuspto-grants-2003_10