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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 216627Generated: October 30, 2026

Sodium Bicarbonate → 2-Aminocarbonylamino-6-(4-hydroxymethylpyridin-2-yl)indole-3-carboxamide

https://huagongshe.com/reaction/216627

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant(2-Bromopyridin-4-yl)methanolHCID 14512957—
Reactant2-Aminocarbonylamino-3-carbamoylindole-6-boronic acid pinacol esterHCID 59189750—
CatalystHCID 178418397HCID 178418397—
Solvent1,4-Dioxane--water (1/1)HCID 21886435—
SolventSodium chloride; waterHCID 57417360—
Product2-Aminocarbonylamino-6-(4-hydroxymethylpyridin-2-yl)indole-3-carboxamideHCID 5918991423.6%

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution mixture of 2-aminocarbonylamino-3-carbamoylindole-6-boronic acid pinacol ester (Compound 6-1, 90 mg, 0.26 mmol), sodium hydrogen carbonate (55 mg, 0.65 mmol), 2-bromopyridine-4-methanol (58 mg, 0.31 mmol) and tetrakis(triphenylphosphine)palladium (0) (15 mg, 0.013 mmol) in water-1,4-dioxane (1:3, 15 mL) was stirred at 100° C. for 6 hours. Brine (5 mL) was added to the reaction mixture, and the whole was extracted with ethyl acetate (5 mL). The organic layer was dried over anhydrous magnesium sulfate, and was filtered throught Celite® pad. After the solvent was evaporated under reduced pressure, the resultant solid was washed with ethanol (2 mL), and dried under reduced pressure to give the title compound (20 mg) as a brown solid (yield 23%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193237B2
Source datasetuspto-grants-2012_06
ORD IDord-254dc5bafe4a48ddaa493831133fd402
Source noteuspto-grants-2012_06