Hydrochloric Acid → HCID 178420508, compound
Reaction equation
[N-:1]=[N+:2]=[N-:3].[Na+].[Al](Cl)(CC)CC.[O:11]([C:18]1[C:27]2[CH:28]=[CH:29][S:30][C:26]=2[C:25]2[CH:24]=[CH:23][C:22]([C:31]#[N:32])=[CH:21][C:20]=2[N:19]=1)[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.[Al](N=[N+]=[N-])(CC)CC.[OH-].[Na+].N([O-])=O.[Na+].Cl>>[O:11]([C:18]1[C:27]2[CH:28]=[CH:29][S:30][C:26]=2[C:25]2[CH:24]=[CH:23][C:22]([C:31]3[NH:32][N:3]=[N:2][N:1]=3)=[CH:21][C:20]=2[N:19]=1)[C:12]1[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=1Participants
Procedure
In an oven dried flask, under nitrogen atmosphere, was charged sodium azide (1.4 eq, 84 mg). Et2AlCl (1.4 eq, 1.08 ml of 1.8 M solution in toluene) was added through syringe. The mixture was stirred at room temperature for 4 hours. 4-phenoxythieno[3,2-c]quinoline-7-carbonitrile (1.0 eq, 20 mg) was charged in a vial. Et2AlN3 solution (0.15 ml) was added and the resulting mixture stirred at 80° C. for 5 days. The mixture was treated by a solution of NaOH and some sodium nitrite was added (pH=13-14). The pH was adjusted to 1.5 with HCl 6N. The material was extracted with ethyl acetate. The material was extracted from the organic phase using a saturated aqueous solution of K2CO3. The pH was adjusted to 2.5 with HCl 6N and the material was extracted with ethyl acetate. The solvent were evaporated to afford 4-phenoxy-7-(1H-tetrazol-5-yl)thieno[3,2-c]quinoline. LCMS (ES)>95% pure, m/z 303 [M+1]+.
Workup
- customIn an oven dried flask
- stirringthe resulting mixture stirred at 80° C. for 5 days
- extractionThe material was extracted with ethyl acetate
- extractionThe material was extracted from the organic phase
- extractionthe material was extracted with ethyl acetate
- customThe solvent were evaporated
Sources & evidence
- ORD record
- ord-1204382e35014fb7b0336f0aed4e85bc
- Source dataset
- uspto-grants-2012_05
- Patent number
- US08168651B2
Reaction notes
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