Tert-butyl 2-(4-aminocyclohexoxy)acetate → tert-butyl 2-[4-[[5-(N-phenylmethoxycarbonylcarbamimidoyl)-1-benzofuran-2-carbonyl]amino]cyclohexyl]oxyacetate
Reaction equation
[CH2:1]([c:2]1[cH:3][cH:4][cH:5][cH:6][cH:7]1)[O:8][C:9](=[O:10])[NH:11][C:12](=[NH:13])[c:14]1[cH:15][cH:16][c:17]2[c:18]([cH:19][c:20]([C:22](=[O:23])[OH:24])[o:21]2)[cH:25]1.[NH2:26][CH:27]1[CH2:28][CH2:29][CH:30]([O:33][CH2:34][C:35](=[O:36])[O:37][C:38]([CH3:39])([CH3:40])[CH3:41])[CH2:31][CH2:32]1>>[CH2:1]([c:2]1[cH:3][cH:4][cH:5][cH:6][cH:7]1)[O:8][C:9](=[O:10])[NH:11][C:12](=[NH:13])[c:14]1[cH:15][cH:16][c:17]2[c:18]([cH:19][c:20]([C:22](=[O:24])[NH:26][CH:27]3[CH2:28][CH2:29][CH:30]([O:33][CH2:34][C:35](=[O:36])[O:37][C:38]([CH3:39])([CH3:40])[CH3:41])[CH2:31][CH2:32]3)[o:21]2)[cH:25]1Participants
3
Sources & evidence
- ORD record
- ord-67e6d8cf77424a16aae8597cfe1f7131
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (10/10)
Reaction notes
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