Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Homoveratrylamine | HCID 8421 | — |
| Reactant | HCID 86748084 | HCID 86748084 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19007105 | HCID 19007105 | 51% |
Reaction Steps
50 ml of a tetrahydrofuran solution containing 4.58 g of N-(2-paratoluenesulfonyloxypropyl)-8-chloro-5-quinolinesulfonamide and 4.95 g of 3,4-dimethoxyphenethylamine was heated at 70° C. for 8 hours in a sealed vessel. Then, the solvent was removed by distillation under reduced pressure to obtain a residue. The thus obtained residue was subjected to purification by silica gel column chromatography [Wacogel C-200, 200 g; solvent: a mixture of methanol and chloroform (5% methanol)] to obtain 2.37 g of N-[2-(3,4-dimethoxyphenethylamino)-2-methylethyl]-8-chloro-5-quinolinesulfonamide (60) (yield: 51%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05340811 |
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| Source dataset | uspto-grants-1994_08 |
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| ORD ID | ord-266bcdc111dc4dbbab30a9fe89bcbbc8 |
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| Source note | uspto-grants-1994_08 |
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