Ethyl 2-bromoisovalerate → HCID 178454940, compound
Reaction equation
[CH:1]1([N:7]([C@H:19]2[CH2:24][CH2:23][C@H:22]([CH3:25])[CH2:21][CH2:20]2)[C:8]([NH:10][C:11]2[S:12][C:13]([S:16]C#N)=[CH:14][N:15]=2)=[O:9])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.SC[C@@H]([C@@H](CS)O)O.C([O:36][C:37](=[O:43])[CH:38](Br)[CH:39]([CH3:41])[CH3:40])C>>[CH:1]1([N:7]([C@H:19]2[CH2:20][CH2:21][C@H:22]([CH3:25])[CH2:23][CH2:24]2)[C:8](=[O:9])[NH:10][C:11]2[S:12][C:13]([S:16][CH:38]([CH:39]([CH3:40])[CH3:41])[C:37]([OH:36])=[O:43])=[CH:14][N:15]=2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1Participants
4
Procedure
Prepared as described in general procedure (H) using 1-cyclohexyl-1-(trans-4-methyl-cyclohexyl)-3-(5-thiocyanato-thiazol-2-yl)-urea, dithioerythritol and ethyl-2-bromoisovalerate.
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-2c1933127f5444a0bbbec0a05b5e240d
- Source dataset
- uspto-grants-2012_09
- Patent number
- US08263634B2
Reaction notes
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