Triethylamine → HCID 178479927, compound
Reaction equation
[I-:1].[CH3:2][N+:3]1[C:8]2[CH:9]=[CH:10][S:11][C:7]=2[C:6](SC)=[N:5][C:4]=1[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1.[I-].[CH3:21][C:22]1[S:23][C:24]2[CH:31]=[CH:30][CH:29]=[CH:28][C:25]=2[N+:26]=1[CH3:27].C(N(CC)CC)C>CN(C)C=O>[I-:1].[CH3:27][N+:26]1[C:25]2[CH:28]=[CH:29][CH:30]=[CH:31][C:24]=2[S:23][C:22]=1[CH:21]=[C:6]1[N:5]=[C:4]([C:14]2[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=2)[N:3]([CH3:2])[C:8]2[CH:9]=[CH:10][S:11][C:7]1=2Participants
5
Conditions
- Temperature
- 80 °C
Procedure
200 mg (0.50 mmol) 1-Methyl-4-methylsulfanyl-2-phenyl-thieno(3,2-d)pyrimidin-1-ium iodide and 145 mg (0.50 mmol) 2,3-dimethyl-benzothiazol-3-ium iodide were dissolved in 2.0 ml dimethylformamide and 202 mg (0.28 ml, 2.00 mmol) triethylamine were added. The green solution was stirred for 1 h at 80° C., filtrated and the residue was washed with methanol. The crude product was purified further by HPLC.
Workup
- filtrationfiltrated
- washthe residue was washed with methanol
- customThe crude product was purified further by HPLC
Sources & evidence
- ORD record
- ord-0b7bf2fe6bb64c30b153690c4d80d56b
- Source dataset
- uspto-grants-2011_11
- Patent number
- US08058431B2
Reaction notes
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