Cyclohexanol → HCID 53633031, compound
Reaction equation
[C:1]1([C:7]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)([CH3:13])[C:8]([N:10]=[C:11]=[O:12])=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH:20]1([OH:26])[CH2:25][CH2:24][CH2:23][CH2:22][CH2:21]1>>[CH:20]1([O:26][C:11](=[O:12])[NH:10][C:8](=[O:9])[C:7]([C:1]2[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=2)([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[CH3:13])[CH2:25][CH2:24][CH2:23][CH2:22][CH2:21]1Participants
3
Procedure
The title compound, white solid, m.p.=126° C. and MS: m/e=351.4 (M+H+) was prepared in accordance with the general method of example 1 from 2,2-diphenylpropionyl isocyanate and cyclohexanol.
Sources & evidence
- ORD record
- ord-3398c2cdbf114e10aefb41bd890a80a7
- Source dataset
- uspto-grants-2003_07
- Patent number
- US06596743B2
Reaction notes
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