Acetone → HCID 152746407, compound
Reaction equation
[Na].CC(C)=O.Cl.[C:7]([NH2:13])(=[NH:12])[CH2:8][CH2:9][CH2:10][CH3:11].[N+:14]([C:17]1[CH:18]=[C:19]([N:23]=[C:24]=[O:25])[CH:20]=[CH:21][CH:22]=1)([O-:16])=[O:15]>C1C=CC=CC=1>[N+:14]([C:17]1[CH:18]=[C:19]([NH:23][C:24]([NH:12][C:7](=[NH:13])[CH2:8][CH2:9][CH2:10][CH3:11])=[O:25])[CH:20]=[CH:21][CH:22]=1)([O-:16])=[O:15]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
Following a procedure similar to that described in Example 1 but using 2.3 g. sodium in 150 ml. dry acetone, 13.6 g. valeramidine hydrochloride, and 16.4 g. 3-nitrophenyl isocyanate in 300 ml. benzene, there was obtained after recrystallization from ethyl alcohol-ether 11.6 g. of the hydrochloride of 1-(3-nitrophenyl)-3-(pentanimidoyl)urea; m.p. 161°-163°C.
Workup
- customafter recrystallization from ethyl alcohol-ether 11.6 g
Sources & evidence
- ORD record
- ord-5dd8b19e973e4aae9b59a52fe4e25382
- Source dataset
- uspto-grants-1976_10
- Patent number
- US03984467
Reaction notes
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