Triethylamine → HCID 178487131, compound
Reaction equation
[I-:1].[CH3:2][O:3][C:4]1[CH:5]=[C:6]2[C:11](=[CH:12][CH:13]=1)[N+:10]([CH3:14])=[C:9]([C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)[N:8]=[C:7]2SC.[I-].[CH3:24][C:25]1[S:26][C:27]2[CH:34]=[CH:33][CH:32]=[CH:31][C:28]=2[N+:29]=1[CH3:30].C(N(CC)CC)C>CN(C)C=O>[I-:1].[CH3:2][O:3][C:4]1[CH:5]=[C:6]2[C:11](=[CH:12][CH:13]=1)[N:10]([CH3:14])[C:9]([C:15]1[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=1)=[N:8][C:7]2=[CH:24][C:25]1[S:26][C:27]2[CH:34]=[CH:33][CH:32]=[CH:31][C:28]=2[N+:29]=1[CH3:30]Participants
5
Conditions
- Temperature
- 80 °C
Procedure
600 mg (1.41 mmol) 6-Methoxy-1-methyl-4-methylsulfanyl-2-phenyl-quinazolin-1-ium iodide and 412 mg (1.41 mmol) 2,3-dimethyl-benzothiazol-3-ium iodide were dissolved in 2.0 ml dimethylformamide and 571 mg (0.79 ml, 5.64 mmol) triethylamine were added. The solution was stirred for 1 h at 80° C., filtrated and the residue was washed with water and methanol.
Workup
- filtrationfiltrated
- washthe residue was washed with water and methanol
Sources & evidence
- ORD record
- ord-9dbb1509a7de4c78bf1a64fe3468fc34
- Source dataset
- uspto-grants-2011_11
- Patent number
- US08058431B2
Reaction notes
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