HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1014321Generated: October 28, 2026
Potassium Carbonate → HCID 59441921, compound
https://huagongshe.com/reaction/1014321
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Isopropylpiperazine | HCID 78013 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Bromoacetyl chloride | HCID 89602 | — |
| Reactant | 5-methoxy-6-nitro-2,3-dihydro-1H-indole | HCID 59441656 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59441921 | HCID 59441921 | 64.4% |
Reaction Steps
To a solution of 5-(methyloxy)-6-nitro-2,3-dihydro-1H-indole (0.5 g, 2.57 mmols) and polymer-bound diisopropyl ethylamine (2.10 g, 7.73 mmol) in dichloromethane (50 mL) was added bromoacetyl chloride (0.49 g, 3.11 mmol) via a dropwise addition. After stirring for two hrs at room temperature, the solids were removed by vacuum filtration. The filtrate was concentrated under reduced pressure, maintained under high vacuum for several hours, redissolved in THF (20 mL) and to this crude mixture was added potassium carbonate (1.06 g, 7.68 mmols), catalytic Kl, and isopropyl piperazine (0.99 g, 7.68 mmols). After overnight stirring, the reaction was diluted with dichloromethane (50 mL), washed with water (25 mL), filtered through a cotton plug and concentrated by rotary evaporation to provide 1-{[4-(1-methylethyl)-1-piperazinyl]acetyl}-5-(methyloxy)-6-nitro-2,3-dihydro-1H-indole (0.60 g, 64% yield). ESIMS (M+H)+=363.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07981903B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-3a1aa37016fa4f31b67e8cc75b5d9805 |
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| Source note | uspto-grants-2011_07 |
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