Hydrochloric Acid → HCID 10943925, compound
Reaction equation
[N:1]1[CH:2]=[C:3]2[N:12]3[C:7](=[CH:8][CH:9]=[CH:10][C:11]=13)[S:6][C:5]([C:13]([O:15]CC)=[O:14])=[CH:4]2.[OH-].[Na+].Cl>C(O)C.O>[N:1]1[CH:2]=[C:3]2[N:12]3[C:7](=[CH:8][CH:9]=[CH:10][C:11]=13)[S:6][C:5]([C:13]([OH:15])=[O:14])=[CH:4]2Participants
6
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
To a solution of 193.69 g of the above ethyl 5-thia-1,8b-diazaacenaphthylene-4-carboxylate in 1 l of ethanol was added a solution of 62.9 g (1.57 mol) of sodium hydroxide in 500 ml of water, and the mixture was stirred at room temperature for 0.5 hour. To this reaction mixture was added about 130 ml of concentrated hydrochloric acid with stirring to bring the pH into the range of 4-5 and the resulting precipitate was recovered by filtration and rinsed with ethanol, acetone, and diethyl ether in that order to provide the title compound.
Workup
- stirringwith stirring
- filtrationthe resulting precipitate was recovered by filtration
- washrinsed with ethanol, acetone, and diethyl ether in that order
Sources & evidence
- ORD record
- ord-6b8f6e72fec547ecb0c5d15aec05b0c7
- Source dataset
- uspto-grants-2001_05
- Patent number
- US06235731B1
Reaction notes
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