Sodium Hydroxide → HCID 12724764, compound
Reaction equation
[Cl:1][C:2]1[CH:11]=[CH:10][C:9]2[N:8]([CH3:12])[C:7]3=[CH:13][C:14]([C:16]([O:18]CC)=[O:17])=[N:15][N:6]3[C:5](=[O:21])[C:4]=2[CH:3]=1.[OH-].[Na+]>CO>[Cl:1][C:2]1[CH:11]=[CH:10][C:9]2[N:8]([CH3:12])[C:7]3=[CH:13][C:14]([C:16]([OH:18])=[O:17])=[N:15][N:6]3[C:5](=[O:21])[C:4]=2[CH:3]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
From 0.6 g of 7-chloro-4,9-dihydro-4-methyl-9-oxo-pyrazolo[5,1-b]quinazoline-2-carboxylic acid, ethyl ester, 22 ml of 0.1 N aqueous sodium hydroxide and 66 ml of methanol, following the procedure of Example 14, there is obtained 7-chloro-4,9-dihydro-4-methyl-9-oxo-pyrazolo[5,1-b]quinazoline-2-carboxylic acid; mp 280° C., after crystallization from dimethylformamide/methanol.
Sources & evidence
- ORD record
- ord-b5ea55fd2984482e8a6b7e1ff111a3a3
- Source dataset
- uspto-grants-1981_04
- Patent number
- US04261997
Reaction notes
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