4-Biphenylyl isocyanate → HCID 22049172, compound
Reaction equation
[NH2:1][CH2:2][CH2:3][N:4]1[CH2:9][CH2:8][CH:7]([C:10]2[CH:11]=[C:12]([NH:16][C:17](=[O:21])[CH:18]([CH3:20])[CH3:19])[CH:13]=[CH:14][CH:15]=2)[CH2:6][CH2:5]1.[CH:22]1[CH:27]=[CH:26][C:25]([C:28]2[CH:33]=[CH:32][C:31]([N:34]=[C:35]=[O:36])=[CH:30][CH:29]=2)=[CH:24][CH:23]=1>C1COCC1>[C:28]1([C:25]2[CH:24]=[CH:23][CH:22]=[CH:27][CH:26]=2)[CH:29]=[CH:30][C:31]([NH:34][C:35]([NH:1][CH2:2][CH2:3][N:4]2[CH2:9][CH2:8][CH:7]([C:10]3[CH:11]=[C:12]([NH:16][C:17](=[O:21])[CH:18]([CH3:19])[CH3:20])[CH:13]=[CH:14][CH:15]=3)[CH2:6][CH2:5]2)=[O:36])=[CH:32][CH:33]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Prepared by Procedure Q1 (THF) and Scheme AT using N-{3-[1-(2-aminoethyl)-4-piperidinyl]phenyl}-2-methylpropanamide and 4-biphenyl isocyanate: ESMS m/e: 485.2 (M+H)+.
Sources & evidence
- ORD record
- ord-bee44c1175184fb098039419a39c05b7
- Source dataset
- uspto-grants-2006_06
- Patent number
- US07067534B1
Reaction notes
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