Ethylamine → HCID 12284406, compound
Reaction equation
[CH3:1][N:2]1[CH:7]=[C:6]([C:8]2[CH:9]=[C:10]([C:14]([F:17])([F:16])[F:15])[CH:11]=[CH:12][CH:13]=2)[C:5](=[O:18])[N:4]=[CH:3]1.[CH2:19](N)C>CO>[CH2:1]([N:2]1[CH:7]=[C:6]([C:8]2[CH:9]=[C:10]([C:14]([F:15])([F:17])[F:16])[CH:11]=[CH:12][CH:13]=2)[C:5](=[O:18])[N:4]=[CH:3]1)[CH3:19]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Two g. of the intermediate atropamide of Example 2 was reacted with 1 cc. of 20 percent aqueous ethylamine in 20 ml. of methanol. The reaction mixture was stirred at reflux temperature for 6 hours and evaporated to dryness, and the residue was recrystallized from ethyl acetatehexane. The product was 1.3 g. of 1-ethyl-5-(α,α,α-trifluoro-m-tolyl)-4(1H)-pyrimidinone, m.p. 172°-173° C.
Workup
- temperatureat reflux temperature for 6 hours
- customevaporated to dryness
- customthe residue was recrystallized from ethyl acetatehexane
Sources & evidence
- ORD record
- ord-90c1838459654ed4931fbbf3ec2e23b8
- Source dataset
- uspto-grants-1977_03
- Patent number
- US04012388
Reaction notes
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