Thiourea → HCID 54190067, compound
Reaction equation
Br.Br[CH:3]1[CH2:9][CH2:8][N:7]([CH2:10][C:11]#[C:12][C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH2:6][CH2:5][C:4]1=O.[NH2:20][C:21]([NH2:23])=[S:22]>C(O)C>[NH2:23][C:21]1[S:22][C:4]2[CH2:5][CH2:6][N:7]([CH2:10][CH:11]=[CH:12][C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)[CH2:8][CH2:9][C:3]=2[N:20]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Prepared from 5-bromo-1-(3-phenyl-2-propyn-1-yl)-hexahydro-4H-azepin-4-one hydrobromide by reacting with thiourea in ethanol. Yield: 4% of theory, Melting point: 145°-148° C.
Sources & evidence
- ORD record
- ord-466458c1c2204cd88cb31c693ab04a75
- Source dataset
- uspto-grants-1991_11
- Patent number
- US05068325
Reaction notes
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