HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 862017Generated: October 28, 2026
Methanol → 6-(Decanoylamino)-1H-indole-4-carboxylic acid
https://huagongshe.com/reaction/862017
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 18800944 | HCID 18800944 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-(Decanoylamino)-1H-indole-4-carboxylic acid | HCID 18800947 | 60.7% |
Reaction Steps
Five hundred-fifteen mg of 4-carbomethoxy-6-(N-decanoylamino)indole [prepared by the method of Wender et al., PNAS, 83: 4214-4218 (1986)] was dissolved in 60 mL of tetrahydrofuran. This solution was treated with 3 mL of a 1N KOH solution in water and also with 5 mL of methanol. The mixture was heated at 80° C. for 32 h. During this period another 2.5 mL of 1N KOH was added in two portions. After cooling the mixture was concentrated in vacuo. The mixture was then diluted with water and acidified with concentrated hydrochloric acid. The mixture was then extracted with methylene chloride. The organic layers were dried over sodium sulfate and concentrated to afford 300 mg of 4-carboxy-6-(N-decanoylamino)indole (60% yield), mp 248°-50 ° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05716968 |
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| Source dataset | uspto-grants-1998_02 |
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| ORD ID | ord-3e38ad870c83435ba103874a45dcb16b |
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| Source note | uspto-grants-1998_02 |
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