HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1992453Generated: October 30, 2026
1-Isopropylpiperazine → 5-(4-Isopropyl-piperazine-1-carbonyl)-1H-indole-2-carboxylic acid ethyl ester
https://huagongshe.com/reaction/1992453
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Isopropylpiperazine | HCID 78013 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| Reactant | 2-(Ethoxycarbonyl)-1H-indole-5-carboxylic acid | HCID 18071365 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-(4-Isopropyl-piperazine-1-carbonyl)-1H-indole-2-carboxylic acid ethyl ester | HCID 68534134 | 74.8% |
Reaction Steps
To a solution of 5.0 g (21.4 mmol) 1H-indole-2,5-dicarboxylic acid 2-ethyl ester (prepared according to J. Org. Chem. 1953, 18, 345-57) in 50 mL N,N-dimethylformamide, were added 8.6 g (26.8 mmol) O-(benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium tetrafluoroborate. After 10 min., 3.44 g (26.8 mmol) 1-isopropylpiperazine and 18.3 mL (13.9 g, 107.4 mmol) N,N-diisopropylethylamine were added. After 45 min. the reaction mixture was poured into saturated aqueous sodium bicarbonate solution and extracted three times with ethyl acetate. The combined organic layers were washed three times with water, brine, dried over magnesium sulfate, filtered and evaporated. The residue was flash-chromatographed on silica gel with dichloromethane:methanol:ammonia (9:1:0.1 v/v) and ethyl acetate:methanol (9:1) as eluant to give 5.5 g (74%) of the desired compound as a light yellow solid. MS (ISP): 344.3 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07648979B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-ff208bc0d7844337b08afc65f1e9b776 |
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| Source note | uspto-grants-2010_01 |
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