Cyclohexanecarbonyl chloride → HCID 53303634, compound
Reaction equation
[C:1]([NH:9][C:10]1[CH:15]=[CH:14][C:13]([C:16]2[CH:24]=[C:23]3[C:19]([CH2:20][N:21]([C@@H:26]([CH:31]([CH3:33])[CH3:32])[C:27]([O:29][CH3:30])=[O:28])[C:22]3=[O:25])=[CH:18][CH:17]=2)=[CH:12][CH:11]=1)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.NC1C=CC(C2C=C3C(CN([C@@H](C(C)C)C(OC)=O)C3=O)=CC=2)=CC=1.C1(C(Cl)=O)CCCCC1>>[CH:2]1([C:1]([NH:9][C:10]2[CH:15]=[CH:14][C:13]([C:16]3[CH:24]=[C:23]4[C:19]([CH2:20][N:21]([C@@H:26]([CH:31]([CH3:33])[CH3:32])[C:27]([O:29][CH3:30])=[O:28])[C:22]4=[O:25])=[CH:18][CH:17]=3)=[CH:12][CH:11]=2)=[O:8])[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7]1Participants
4
Procedure
The compound of example 117 was prepared analogous to compound of example 97 by reaction of compound of example 6 with cyclohexoyl chloride.
Sources & evidence
- ORD record
- ord-af15882de0964f148304783e2f2e875f
- Source dataset
- uspto-grants-2014_06
- Patent number
- US08748426B2
Reaction notes
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