HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 3579Generated: October 25, 2026
Triethylamine → N-[4-(Pyrrolo[1,2-a]quinoxalin-5(4H)-ylcarbonyl)phenyl]-2,3-dichlorobenzamide
https://huagongshe.com/reaction/3579
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,3-Dichlorobenzoyl chloride | HCID 17944 | — |
| Reactant | 4,5-Dihydro-5-(4-aminobenzoyl)pyrrolo[1,2-a]quinoxaline | HCID 21837005 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-[4-(Pyrrolo[1,2-a]quinoxalin-5(4H)-ylcarbonyl)phenyl]-2,3-dichlorobenzamide | HCID 21837108 | 13.3% |
Reaction Steps
As described for Example 157, 0.47 g of 4,5-dihydro-5-(4-aminobenzoyl)pyrrolo[1,2-a]quinoxaline, 346 μl of triethylamine and 5 ml of dichloromethane are chilled (ice bath) and 0.415 g of 2,3-dichlorobenzoyl chloride in 2 ml of dichloromethane added. After stirring overnight, an additional 346 μl of triethylamine is added and an additional 0.415 g of 2,3-dichlorobenzoyl chloride added. The mixture is stirred for 2 hours, diluted with 50 ml of dichloromethane and the solution washed with 20 ml each of H2O, 2N citric acid, 1M NaHCO3 and brine. The organic layer is dried (Na2SO4) and filtered through a thin pad of hydrous magnesium silicate and the filtrate concentrated to dryness. The residue is chromatographed on thick layer silica gel plates with ethyl acetate-hexane (1:1) as solvent to give 0.100 g of white solid, m.p. 230°-240° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05733905 |
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| Source dataset | uspto-grants-1998_03 |
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| ORD ID | ord-19075005e7214f38bc08e67939d9a779 |
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| Source note | uspto-grants-1998_03 |
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