Oxalic acid dihydrate → HCID 19388576, compound
Reaction equation
[C:1]([OH:6])(=[O:5])[C:2]([OH:4])=[O:3].O.O.[CH2:9]([N:16]1[C:25]2[C:20](=[CH:21][C:22]([Cl:26])=[CH:23][CH:24]=2)[C:19](=[O:27])[N:18]([CH2:28][CH2:29][N:30]([CH2:33][CH3:34])[CH2:31][CH3:32])[CH2:17]1)[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1>C(OCC)C.C(O)C>[C:1]([OH:6])(=[O:5])[C:2]([OH:4])=[O:3].[CH2:9]([N:16]1[C:25]2[C:20](=[CH:21][C:22]([Cl:26])=[CH:23][CH:24]=2)[C:19](=[O:27])[N:18]([CH2:28][CH2:29][N:30]([CH2:33][CH3:34])[CH2:31][CH3:32])[CH2:17]1)[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
763 Milligrammes (6.1 mmoles) of dihydrate oxalic acid dissolved in 20 ml of a mixture of ethyl ether-ethyl alcohol in a ratio of 5:1 are added to 2.00 grammes (6.1 mmoles) of 1-benzyl-6-chloro-3-[2-(diethylamino)ethyl]-2,3-dihydro-4(1H)-quinazolinone and the product, which immediately crystallizes, is recovered through filtration with a yield of 50%. The product obtained has the following chemical-physical characteristics:
Workup
- customthe product, which immediately crystallizes
- filtrationis recovered through filtration with a yield of 50%
- customThe product obtained
Sources & evidence
- ORD record
- ord-b41137e1343d47b099c3512fceafa79e
- Source dataset
- uspto-grants-1995_08
- Patent number
- US05446152
Reaction notes
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