HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1836142Generated: October 30, 2026
Potassium Carbonate → HCID 23498835, compound
https://huagongshe.com/reaction/1836142
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methanol--water (1/1) | HCID 22242641 | — |
| Reactant | acetic acid 2-{4-[3-(2-formyl-4,5,6,7-tetrahydro-1H-indol-3-yl)-propyl]-piperazin-1-yl}-2-oxo-ethyl ester | HCID 86588563 | — |
| Solvent | Dichloromethane methanol | HCID 21226129 | — |
| Product | HCID 23498835 | HCID 23498835 | — |
Reaction Steps
Each fraction of acetic acid 2-{4-[3-(2-formyl-4,5,6,7-tetrahydro-1H-indol-3-yl)-propyl]-piperazin-1-yl}-2-oxo-ethyl ester was treated separately with potassium carbonate (3.0 eq.) in 6 ml of (methanol/ water 4/1). The two reactions were stirred at room temperature for overnight. Thin layer chromatography (dichloromethane: methanol 15:1) for both reactions showed the same spot and also LCMS showed that they have the same molecular weight. The two reactions were combined and the solvent was evaporated. The formed solid was washed with 30 ml of (dichloromethane/methanol 10/1) three times and sonicated. The liquid was collected and concentrated to give 268 mg of 3-{3-[4-(2-hydroxyacetyl)piperazin-1-yl]-propyl}-4,5,6,7-tetrahydro-1H-indole-2-carbaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06777417B2 |
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| Source dataset | uspto-grants-2004_08 |
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| ORD ID | ord-3ac57756a19544f3b35f9fb782d83361 |
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| Source note | uspto-grants-2004_08 |
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