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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (2-Bromopyridin-4-yl)methanol | HCID 14512957 | — |
| Reactant | 2-Aminocarbonylamino-3-carbamoylindole-6-boronic acid pinacol ester | HCID 59189750 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,4-Dioxane--water (1/1) | HCID 21886435 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 2-Aminocarbonylamino-6-(4-hydroxymethylpyridin-2-yl)indole-3-carboxamide | HCID 59189914 | 23.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08193237B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-254dc5bafe4a48ddaa493831133fd402 |
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| Source note | uspto-grants-2012_06 |
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