Hydrochloric Acid → HCID 12535845, compound
Reaction equation
[O:1]=[C:2]1[NH:7][C:6]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=2[O:14][CH:15]([CH3:17])[CH3:16])=[N:5][CH:4]=[C:3]1[C:18]([O:20]CC)=[O:19].Cl>[OH-].[Na+]>[O:1]=[C:2]1[NH:7][C:6]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=2[O:14][CH:15]([CH3:17])[CH3:16])=[N:5][CH:4]=[C:3]1[C:18]([OH:20])=[O:19]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of ethyl 1,6-dihydro-6-oxo-2-(2-isopropoxyphenyl)pyrimidine-5-carboxylate (3.02 g.) in 1N NaOH (25 ml.) was heated on a steam bath for 15 minutes. The solution was acidified with 1N HCl (26 ml.) to precipitate 2.7 g. of the title acid, m.p. 191°-193°. Recrystallization from methanol gave pale yellow crystals of the acid, m.p. 193°-195°.
Workup
- customto precipitate 2.7 g
- customRecrystallization from methanol
- customgave pale yellow crystals of the acid, m.p. 193°-195°
Sources & evidence
- ORD record
- ord-3ffce8a1b5714b87a91d0a115d57334c
- Source dataset
- uspto-grants-1977_06
- Patent number
- US04031093
Reaction notes
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