HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1383334Generated: October 31, 2026
Tetrahydrofuran → 4-(4-Methylpiperazin-1yl)indole-2-carboxylic acid
https://huagongshe.com/reaction/1383334
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Lithium hydroxide, monohydrate | HCID 168937 | — |
| Reactant | 1-(2-(ethoxycarbonyl)-1H-indol-4-yl)-4-methylpiperazine | HCID 15550245 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(4-Methylpiperazin-1yl)indole-2-carboxylic acid | HCID 21187590 | 49% |
Reaction Steps
A solution of 1-(2-(ethoxycarbonyl)-1H-indol-4-yl)-4-methylpiperazine (0.91 g, 3.17 mmol), lithium hydroxide hydrate (0.136 g, 3.17 mmol, 1.0 equivalent), tetrahydrofuran (20 mL), and water (4 mL) was heated at reflux under nitrogen for 16 hours. The resulting reaction mixture was evaporated under reduced pressure, and the residue was chromatographed using silica gel (approximately 30 g) and elution with methylene chloride/methanol/ammonium hydroxide [3:2:0.2] to afford the title compound (0.40 g, 1.54 mmol, 49%) as a white solid: mp, 272-273° C.; R, =0.05 in methylene chloride/methanol/ammonium hydroxide [5:1:0.1]; 13C NMR (D2O) δ169.4, 145.0, 137.5, 132.9, 124.7, 120.7, 108.2, 107.3, 103.7, 58.7, 53.7, 51.0; LRMS (m/z, relative intensity) 260 (18), 259 (M+, 100), 244 (9), 215 (7), 170 (24); HRMS calculated for C14H17N3O2 259.1322, found 259.1325.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06255306B1 |
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| Source dataset | uspto-grants-2001_07 |
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| ORD ID | ord-e5ceba4b334244c2ab903fb48b9be35a |
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| Source note | uspto-grants-2001_07 |
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