Hydrochloric Acid → HCID 178428935, compound
Reaction equation
C([O:3][C:4]([C:6]1[C:7]([CH3:32])=[N:8][C:9]([CH3:31])=[CH:10][C:11]=1[O:12][CH2:13][C:14]1[CH:19]=[CH:18][C:17]([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][C:21]=2[C:26]2[NH:30][N:29]=[N:28][N:27]=2)=[CH:16][CH:15]=1)=[O:5])C.Cl>[OH-].[Na+]>[C:4]([C:6]1[C:7]([CH3:32])=[N:8][C:9]([CH3:31])=[CH:10][C:11]=1[O:12][CH2:13][C:14]1[CH:15]=[CH:16][C:17]([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][C:21]=2[C:26]2[NH:30][N:29]=[N:28][N:27]=2)=[CH:18][CH:19]=1)([OH:5])=[O:3]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
150 mg of the compound obtained in Example 40 was dissolved in 2 ml of 1N NaOH. The solution was stirred at 60°-70° C. for 24 hours, and then cooled. The pH of the reaction mixture was adjusted to 3 with 1N HCl. The precipitate obtained was collected by filtration, washed with water, and then dried to give 84 mg of a colorless powder of the title compound (yield: 60%).
Workup
- temperaturecooled
- customThe precipitate obtained
- filtrationwas collected by filtration
- washwashed with water
- customdried
Sources & evidence
- ORD record
- ord-12ba4e7e938347c9bad4ef4c16694f9c
- Source dataset
- uspto-grants-1995_03
- Patent number
- US05399566
Reaction notes
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