Hydrochloric Acid → HCID 178524378, compound
Reaction equation
[NH:1]1[C:5]([C:6]2[CH:7]=[CH:8][C:9]3[C:10]4[S:30][CH:29]=[CH:28][C:11]=4[C:12]([NH:16][C:17]4[CH:18]=[C:19]([CH:25]=[CH:26][CH:27]=4)[C:20]([O:22]CC)=[O:21])=[N:13][C:14]=3[CH:15]=2)=[N:4][N:3]=[N:2]1.C1COCC1.[OH-].[Li+].Cl>O.CO>[NH:1]1[C:5]([C:6]2[CH:7]=[CH:8][C:9]3[C:10]4[S:30][CH:29]=[CH:28][C:11]=4[C:12]([NH:16][C:17]4[CH:18]=[C:19]([CH:25]=[CH:26][CH:27]=4)[C:20]([OH:22])=[O:21])=[N:13][C:14]=3[CH:15]=2)=[N:4][N:3]=[N:2]1Participants
7
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Procedure
ethyl 3-(7-(1H-tetrazol-5-yl)thieno[3,2-c]quinolin-4-ylamino)benzoate (1.0 eq, 7.6 mg, 0.018 mmol) was suspended in a 1:1:1 mixture of THF, MeOH and water. Lithium Hydroxide was added (40 mg, 1.66 mmol) and the mixture stirred at room temperature for one hour. Water and hydrochloric acid were added and the resulting solid filtered and dried to afford 3-(7-(1H-tetrazol-5-yl)thieno[3,2-c]quinolin-4-ylamino)benzoic acid as a solid. LCMS (ES): 95% pure, m/z 389 [M+1]+.
Workup
- filtrationthe resulting solid filtered
- customdried
Sources & evidence
- ORD record
- ord-fadefebc8de44c739fa3a4b0f12af03b
- Source dataset
- uspto-grants-2012_05
- Patent number
- US08168651B2
Reaction notes
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