4-tert-butyl-N-cyclohexylcyclohexan-1-amine → {2-[3-(trans-4-tert-Butyl-cyclohexyl)-3-cyclohexyl-ureido]-thiazol-5-ylsulfanyl}-acetic acid
Reaction equation
[C:28]([CH3:29])([CH3:30])([CH3:31])[CH:32]1[CH2:33][CH2:34][CH:35]([NH:38][CH:39]2[CH2:40][CH2:41][CH2:42][CH2:43][CH2:44]2)[CH2:36][CH2:37]1.[CH2:45]([O:46][C:47](=[O:48])[CH2:49][S:50][c:51]1[s:52][c:53]([NH2:54])[n:55][cH:56]1)[CH3:57].[CH:1]1([N:2]([CH:3]2[CH2:4][CH2:5][CH:6]([CH2:20][CH3:21])[CH2:22][CH2:23]2)[C:7]([NH:8][c:9]2[s:10][c:11]([S:14][CH2:15][C:16](=[O:17])[OH:18])[cH:12][n:13]2)=[O:19])[CH2:24][CH2:25][CH2:26][CH2:27]1>>[C:7]([NH:8][c:9]1[s:10][c:11]([S:14][CH2:15][C:16](=[O:17])[OH:18])[cH:12][n:13]1)(=[O:19])[N:38]([CH:35]1[CH2:34][CH2:33][CH:32]([C:28]([CH3:29])([CH3:30])[CH3:31])[CH2:37][CH2:36]1)[CH:39]1[CH2:40][CH2:41][CH2:42][CH2:43][CH2:44]1Participants
4
Reactant 3
Product 1
Sources & evidence
- ORD record
- ord-f2eedde555d64e0586b9b5d801f04fb1
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (5/10)
Reaction notes
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