HCID 59256646, compound → HCID 136352897, compound
Reaction equation
C([O:8][C:9]1[C:10]([Cl:24])=[CH:11][C:12]([Cl:23])=[C:13]2[C:18]=1[N:17]=[C:16]([CH2:19][N:20]([CH3:22])[CH3:21])[CH:15]=[N:14]2)C1C=CC=CC=1>Cl>[ClH:23].[Cl:24][C:10]1[CH:11]=[C:12]([Cl:23])[C:13]2[N:14]=[CH:15][C:16]([CH2:19][N:20]([CH3:21])[CH3:22])=[N:17][C:18]=2[C:9]=1[OH:8]Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of (8-benzyloxy-5,7-dichloro-quinoxalin-2-ylmethyl)dimethylamine (38 mg, 0.105 mmol) in conc HCl (2 mL) was stirred at room temperature for 16 h. The orange solution was concentrated to dryness and the remaining residue was washed with diethyl ether (2 ml×3) to give the desired product as a light yellow solid (27 mg, 83%).
Workup
- concentrationThe orange solution was concentrated to dryness
- washthe remaining residue was washed with diethyl ether (2 ml×3)
Sources & evidence
- ORD record
- ord-05af723e6c1d47d7a22e58b387018a4f
- Source dataset
- uspto-grants-2010_04
- Patent number
- US07692011B2
Reaction notes
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