Hydrochloric Acid → HCID 19087827, compound
Reaction equation
C([O:4][CH2:5][CH2:6][O:7][C:8]1[CH:9]=[C:10]2[C:15](=[CH:16][CH:17]=1)[N:14]=[C:13]([CH2:18][CH2:19][CH3:20])[N:12]([CH2:21][C:22]1[CH:27]=[CH:26][C:25]([C:28]3[CH:33]=[CH:32][CH:31]=[CH:30][C:29]=3[C:34]3[N:38]([CH2:39][O:40][CH3:41])[N:37]=[N:36][N:35]=3)=[CH:24][CH:23]=1)[C:11]2=[O:42])(=O)C.C1COCC1.[OH-].[Na+].Cl>CO>[OH:4][CH2:5][CH2:6][O:7][C:8]1[CH:9]=[C:10]2[C:15](=[CH:16][CH:17]=1)[N:14]=[C:13]([CH2:18][CH2:19][CH3:20])[N:12]([CH2:21][C:22]1[CH:23]=[CH:24][C:25]([C:28]3[CH:33]=[CH:32][CH:31]=[CH:30][C:29]=3[C:34]3[N:38]([CH2:39][O:40][CH3:41])[N:37]=[N:36][N:35]=3)=[CH:26][CH:27]=1)[C:11]2=[O:42]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 6-(2-acetoxyethyloxy)-3-[[2'-(N-methoxymethyltetrazol-5-yl)biphenyl-4-yl]methyl]-2-propyl-4(3H)-quinazolinone (0.42 g) in a mixture of methanol (3 ml), THF (2 ml) and 1N aqueous sodium hydroxide (1.5 ml) was stirred at room temperature for 1 hour. After addition of 1N hydrochloric acid (1.5 ml), the reaction mixture was extracted with ethyl acetate and the extract was washed with water, dried and evaporated to dryness. The residue was purified by column chromatography on silica gel to give a white powder.
Workup
- extractionthe reaction mixture was extracted with ethyl acetate
- washthe extract was washed with water
- customdried
- customevaporated to dryness
- customThe residue was purified by column chromatography on silica gel
- customto give a white powder
Sources & evidence
- ORD record
- ord-c8c2159efdc641289614d15d6d0be195
- Source dataset
- uspto-grants-1994_04
- Patent number
- US05304565
Reaction notes
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