Sulfuric Acid → HCID 18402914, compound
Reaction equation
[Cl:1][C:2]1[C:7]([O:8][C:9]2[CH:14]=[CH:13][C:12](N)=[CH:11][CH:10]=2)=[CH:6][C:5]([N:16]2[C:21](=[O:22])[CH:20]=[C:19]([C:23]([F:26])([F:25])[F:24])[NH:18][C:17]2=[O:27])=[C:4]([F:28])[CH:3]=1.S(=O)(=O)(O)[OH:30].N([O-])=O.[Na+].NC(N)=O>O.[Cu-]=O>[Cl:1][C:2]1[C:7]([O:8][C:9]2[CH:14]=[CH:13][C:12]([OH:30])=[CH:11][CH:10]=2)=[CH:6][C:5]([N:16]2[C:21](=[O:22])[CH:20]=[C:19]([C:23]([F:25])([F:24])[F:26])[NH:18][C:17]2=[O:27])=[C:4]([F:28])[CH:3]=1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Procedure
3-[4-Chloro-2-fluoro-5-(4-aminophenoxy)phenyl]-6-trifluoromethyl-1,2,3,4-tetrahydro-pyrimidine-2,4-dione (2.0 g) was mixed with hot 30% sulfuric acid (5 ml) and ice/water (5.0 g) was added. The mixture kept at 10° C. while a solution of sodium nitrite (0.45 g) in water (5 ml) was slowly introduced at the bottom of the stirred mixture. After stirring for 10 minutes, urea (0.1 g) was added, followed by a solution of copper(2)nitrate (18.0 g) in water (170 ml), and copper(1)oxide (0.7 g). The mixture was stirred for 10 minutes, extracted with diethyl ether (50 ml×3), and dried over sodium sulfate. The crude product was purified by column chromatography (hexane:ethyl acetate, 4:1) to give 3-[4-chloro-2-fluoro-5-(4-hydroxyphenoxy)phenyl]-6-trifluoromethyl-1,2,3,4-tetrahydropyrimidine-2,4-dione (Intermediate 11-31), (1.0 g).
Workup
- additionwas added
- additionwas slowly introduced at the bottom of the stirred mixture
- stirringThe mixture was stirred for 10 minutes
- extractionextracted with diethyl ether (50 ml×3)
- dry with materialdried over sodium sulfate
- customThe crude product was purified by column chromatography (hexane:ethyl acetate, 4:1)
Sources & evidence
- ORD record
- ord-d89c537ed2bb4316ab853e09a4cf2520
- Source dataset
- uspto-grants-2001_10
- Patent number
- US06303543B1
Reaction notes
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