Ethyl Acetate → HCID 59515870, compound
Reaction equation
[N+:1]([C:4]1[CH:13]=[CH:12][CH:11]=[C:10]2[C:5]=1[CH:6]=[CH:7][N:8]([C@H:15]([CH3:20])[C:16]([O:18]C)=[O:17])[C:9]2=[O:14])([O-:3])=[O:2].[I-].[Li+].C(OCC)(=O)C>>[N+:1]([C:4]1[CH:13]=[CH:12][CH:11]=[C:10]2[C:5]=1[CH:6]=[CH:7][N:8]([C@H:15]([CH3:20])[C:16]([OH:18])=[O:17])[C:9]2=[O:14])([O-:3])=[O:2]Participants
4
Procedure
(R)-Methyl 2-(5-nitro-1-oxoisoquinolin-2(1H)-yl)propanoate (5.2 g, 0.019 mol) and lithium iodide (10 g, 0.08 mol) were refluxed in ethyl acetate (200 mL, 2 mol) for 64 hours. The solid was filtered, and the filtrate was concentrated and gave a brown solid.
Workup
- filtrationThe solid was filtered
- concentrationthe filtrate was concentrated
- customgave a brown solid
Sources & evidence
- ORD record
- ord-f527dcbb4722478a887d9974643ff076
- Source dataset
- uspto-grants-2010_10
- Patent number
- US07816371B2
Reaction notes
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