Hydrochloric Acid → HCID 178524905, compound
Reaction equation
[OH-].[Na+].[CH2:3]([O:10][C:11]1[C:12]([C:18]([O:20]C)=[O:19])=[N:13][CH:14]=[N:15][C:16]=1[OH:17])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.Cl>CO>[CH2:3]([O:10][C:11]1[C:12]([C:18]([OH:20])=[O:19])=[N:13][CH:14]=[N:15][C:16]=1[OH:17])[C:4]1[CH:5]=[CH:6][CH:7]=[CH:8][CH:9]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Methanol (6 ml) and 1N aqueous sodium hydroxide solution (2.5 ml) were added to methyl 5-benzyloxy-6-hydroxypyrimidine-4-carboxylate (530 mg) obtained in the previous step, and the mixture was stirred at room temperature for 1 hr. 2N Hydrochloric acid (2.5 ml) was added to the reaction mixture, and methanol was evaporated under reduced pressure. The precipitate was collected by filtration, washed with water and dried to give 5-benzyloxy-6-hydroxypyrimidine-4-carboxylic acid (253 mg).
Workup
- customobtained in the previous step
- customwas evaporated under reduced pressure
- filtrationThe precipitate was collected by filtration
- washwashed with water
- customdried
Sources & evidence
- ORD record
- ord-669918212c7b436d8a742c97786c0910
- Source dataset
- uspto-grants-2007_05
- Patent number
- US07211572B2
Reaction notes
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