HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1188942Generated: November 2, 2026
Ammonium Hydroxide → HCID 66897826, compound
https://huagongshe.com/reaction/1188942
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | HCID 66897952 | HCID 66897952 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 66897826 | HCID 66897826 | 74% |
Reaction Steps
A mixture of 5-{[6-(methoxymethyl)pyridin-3-yl]oxy}-7-(1-methylethoxy)-1H-indole-2-carboxylic acid (1.43 g), 1-hydroxybenzotriazole (810 mg), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (1.15 g) and N,N-dimethylformamide (50 mL) was stirred at room temperature for 30 min. An aqueous solution of ammonium hydroxide (25%, 5 mL) was added to the mixture. The whole was stirred at room temperature for 4.5 days. Water was added to the mixture and the mixture was extracted with ethyl acetate. The organic layer was washed successively with water, saturated aqueous solution of sodium hydrogen carbonate and brine, dried (MgSO4) filtered, and concentrated in vacuo. The residue was washed with diisopropyl ether to give the title compound (1.05 g, 74%) as pale brown crystals. MS 356 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08673942B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-d1324dca2cc34abd8a1f888cd53fec30 |
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| Source note | uspto-grants-2014_03 |
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