Sulfuric Acid → HCID 18402914, compound

HRID 380313Notes

Reaction equation

HRID 380313 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]=1

Participants

7

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

  1. additionwas added
  2. additionwas slowly introduced at the bottom of the stirred mixture
  3. stirringThe mixture was stirred for 10 minutes
  4. extractionextracted with diethyl ether (50 ml×3)
  5. dry with materialdried over sodium sulfate
  6. 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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