HCID 21098149, compound → HCID 21098099, compound
Reaction equation
[CH3:1][C:2]1[C:11]([CH3:12])=[N:10][C:9]2[C:4](=[C:5]([CH3:17])[CH:6]=[C:7]([C:13](OC)=[O:14])[CH:8]=2)[N:3]=1.[H-].[Al+3].[Li+].[H-].[H-].[H-]>O1CCCC1>[CH3:1][C:2]1[C:11]([CH3:12])=[N:10][C:9]2[C:4](=[C:5]([CH3:17])[CH:6]=[C:7]([CH2:13][OH:14])[CH:8]=2)[N:3]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Prepared by reducing 691 mg of methyl 2,3,8-trimethyl-quinoxaline-6-carboxylate with 300 mg of lithium aluminium hydride (95%) in 15 ml tetrahydrofuran at ambient temperature.
Workup
- customPrepared
- customat ambient temperature
Sources & evidence
- ORD record
- ord-326e2e6e619c403b8a44ca178164fab5
- Source dataset
- uspto-grants-2007_05
- Patent number
- US07217711B2
Reaction notes
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