3-(Trifluoromethyl)phenyl isocyanate → HCID 152746473, compound
Reaction equation
[Na].Cl.[C:3]([NH2:9])(=[NH:8])[CH2:4][CH2:5][CH2:6][CH3:7].[F:10][C:11]([F:22])([F:21])[C:12]1[CH:13]=[C:14]([N:18]=[C:19]=[O:20])[CH:15]=[CH:16][CH:17]=1>CC(C)=O>[F:10][C:11]([F:21])([F:22])[C:12]1[CH:13]=[C:14]([NH:18][C:19]([NH:8][C:3](=[NH:9])[CH2:4][CH2:5][CH2:6][CH3:7])=[O:20])[CH:15]=[CH:16][CH:17]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Following a procedure similar to that described in Example 1 but using 2.3 g. sodium in 250 ml. dry acetone, 13.6 g. valeramidine hydrochloride, and 18.7 g. 3-(trifluoromethyl)phenyl isocyanate in 100 ml. dry acetone, there was obtained after recrystallization from acetonitrile 17.9 g. of the hydrochloride of 1-[3-(trifluoromethyl)phenyl]-3-(pentanimidoyl)urea; m.p. 167°-169°C.
Workup
- customafter recrystallization from acetonitrile 17.9 g
Sources & evidence
- ORD record
- ord-1195822c41214dcb93024c18d617ffb6
- Source dataset
- uspto-grants-1976_10
- Patent number
- US03984467
Reaction notes
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