HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → N-(1,2,3,4-tetrahydro-2-propyl-5-isoquinolinyl)-acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 1-Iodopropane | HCID 33643 | — |
| Reactant | 5-Nitroisoquinoline | HCID 69085 | — |
| Product | N-(1,2,3,4-tetrahydro-2-propyl-5-isoquinolinyl)-acetamide | HCID 10376661 | — |
Reaction Steps
A solution of 5-nitroisoquinoline (25 g, 0.144 mol) and iodopropane (36.7 g, 0.216 mol) in 500 mL of EtOH was converted to the title compound by the procedures described in Example 1. The crude title compound was purified by chromatography (silica gel, 95:5 EtOAc:EtOH). The purified product was recrystallized from iPr2O/THF to give the title compound as a white solid (3.33 g, 18%), mp=123° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06703391B2 |
| Source dataset | uspto-grants-2004_03 |
| ORD ID | ord-6b284eb5fb784751a6f68a70a1b7e4ac |
| Source note | uspto-grants-2004_03 |