HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 219757Generated: October 27, 2026
Pyridine → 3-Amino-5-cyano-3-(2-ethoxyphenyl)indol-2-one
https://huagongshe.com/reaction/219757
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 5-Cyano-3-(2-ethoxyphenyl)-3-hydroxy-indol-2-one | HCID 66593041 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Amino-5-cyano-3-(2-ethoxyphenyl)indol-2-one | HCID 66593070 | 58.9% |
Reaction Steps
8.0 g (27.2 mMol) of intermediate 1b and 43 ml (54.4 mMol) of pyridine were dissolved in 70 ml of methylene chloride. Then, at 0° C., 3 ml (40.8 mMol) of SOCl2 were slowly added dropwise. The reaction mixture was then stirred for a further 30 minutes. The reaction solution was subsequently poured into ice-water, and the organic phase was separated off, washed with water, dried and concentrated in vacuo. This residue was added at 0° C. to a solution of 300 ml of 0.5M NH3 solution in dioxane and 150 ml of methylene chloride. The mixture was stirred at room temperature for 16 h. The reaction solution was concentrated in vacuo, and the residue obtained in this way was suspended in water. The precipitate was separated off and recrystallized from a little methanol. 4.7 g of the product were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08202870B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-65a6d94997b24430b7e1d6ff952ca48c |
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| Source note | uspto-grants-2012_06 |
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