Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 4-Chlorobenzylamine | HCID 66036 | — |
| Reactant | HCID 21192588 | HCID 21192588 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 21192589 | HCID 21192589 | — |
Reaction Steps
To a flask containing ethyl 1-cyclopropyl-6-iodo-4-oxo-1,4-dihydro-3-quinolinecarboxylate from Preparation No. 19 (0.19 g) is added p-chlorobenzylamine (1.0 mL). The reaction is tightly capped and heated to 180° C. for 1 hour. The reaction is cooled to room temperature and partioned between dichloromethane containing methanol and dilute hydrochloric acid. The aqueous layer is extracted with dichloromethane and the combined organic layers are washed with brine, dried and concentarted under reduced pressure. The residue is adsorbed onto silica and chromatographed on silica eluting with 2% to 6% methanol in dichloromethane. The product containing fractions are evaporated to give 0.10 g of the title compound as a tan solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06248739B1 |
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| Source dataset | uspto-grants-2001_06 |
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| ORD ID | ord-481d449fb8a44f689113986e34bac7e4 |
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| Source note | uspto-grants-2001_06 |
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