HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1042142Generated: October 31, 2026
1H-Benzotriazole, 1-hydroxy-, ammonium salt (1:1) → 7-Methyl-5-{[6-(methylsulfonyl)pyridin-3-yl]oxy}-1H-indole-2-carboxamide
https://huagongshe.com/reaction/1042142
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1H-Benzotriazole, 1-hydroxy-, ammonium salt (1:1) | HCID 113175 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | HCID 66726052 | HCID 66726052 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 7-Methyl-5-{[6-(methylsulfonyl)pyridin-3-yl]oxy}-1H-indole-2-carboxamide | HCID 66726141 | 90% |
Reaction Steps
To a solution (35 mL) of 7-methyl-5-{[6-(methylsulfonyl)pyridin-3-yl]oxy}-1H-indole-2-carboxylic acid (3.3 g) in N,N-dimethylformamide were added under ice-cooling 1-hydroxybenzotriazole ammonia salt (2.0 g) and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (2.5 g), and the mixture was stirred from under ice-cooling to room temperature for 15 hr. The reaction solution was concentrated under reduced pressure, water was added to the obtained residue, and the mixture was extracted with ethyl acetate. The organic layer was washed with aqueous sodium hydrogen carbonate solution and saturated brine, dried over magnesium sulfate, filtered and concentrated under reduced pressure. The obtained pale-yellow oil was crystallized from ethyl acetate to give the title compound (2.95 g, yield 90%) as pale-yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08557805B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-566fe506f3ed4fe9b715b4ef3cc01e7a |
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| Source note | uspto-grants-2013_10 |
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