Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Fluorobenzenesulfonyl chloride | HCID 9588 | — |
| Reactant | HCID 68937404 | HCID 68937404 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86627492 | HCID 86627492 | 38% |
Reaction Steps
82 μL (0.59 mmol) of triethylamine is added to 60 mg (0.20 mmol) of 8-amino-4-oxo-4,5-dihydro-3H-pyrrolo[2,3-c]quinoline-1-ethyl carboxylate hydrochloride (synthesis 64) suspended in anhydrous dimethylformamide (1 mL). The mixture is cooled to 0° C., then 42 mg (0.21 mmol) of 4-fluoro-benzenesulfonyl chloride is added. The solution is stirred for 1 h at 0° C. The solvent is evaporated and the raw product obtained is purified by recrystallization from methanol to give 32 mg (38%) of 8-(4-fluoro-benzenesulfonylamino)-4-oxo-4,5-dihydro-3H-pyrrolo[2,3-c]quinoline-1-ethyl carboxylate in the form of a light brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08426437B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-9a157dc093f044debcf8ac1fab4280ef |
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| Source note | uspto-grants-2013_04 |
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