Tert-butyl 5-chlorospiro[indoline-3,3'-pyrrolidine]-1'-carboxylate → tert-butyl 5-chloro-1-[5-methyl-7-(4-nitrobenzoyl)oxy-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-yl]spiro[2H-indole-3,3'-pyrrolidine]-1'-carboxylate
Reaction equation
[Cl:24][c:25]1[cH:26][c:27]2[c:31]([cH:32][cH:33]1)[NH:30][CH2:29][C:28]21[CH2:34][N:35]([C:38](=[O:39])[O:40][C:41]([CH3:42])([CH3:43])[CH3:44])[CH2:36][CH2:37]1.[N+:1](=[O:2])([O-:3])[c:4]1[cH:5][cH:6][c:7]([C:8](=[O:9])[O:10][CH:11]2[CH2:12][CH:13]([CH3:21])[c:14]3[c:15]2[n:16][cH:17][n:18][c:19]3[Cl:20])[cH:22][cH:23]1>>[N+:1](=[O:2])([O-:3])[c:4]1[cH:5][cH:6][c:7]([C:8](=[O:9])[O:10][CH:11]2[CH2:12][CH:13]([CH3:21])[c:14]3[c:15]2[n:16][cH:17][n:18][c:19]3[N:30]2[CH2:29][C:28]3([c:27]4[cH:26][c:25]([Cl:24])[cH:33][cH:32][c:31]42)[CH2:34][N:35]([C:38](=[O:39])[O:40][C:41]([CH3:42])([CH3:43])[CH3:44])[CH2:36][CH2:37]3)[cH:22][cH:23]1Participants
3
Reactant 2
Product 1
Sources & evidence
- ORD record
- ord-4bfbad9f0a1341fcb9d911ed370c0021
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (1/10)
Reaction notes
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