4-(2-Oxa-6-azaspiro[3.3]heptan-6-ylmethyl)-2-chlorophenol → (3-(4-(2-Oxa-6-azaspiro[3.3]heptan-6-ylmethyl)-2-chlorophenoxy)azetidin-1-yl)(5-phenyl-1,3,4-oxadiazol-2-yl)methanone
Reaction equation
[CH2:1]1[O:2][CH2:3][C:4]12[CH2:5][N:6]([CH2:8][c:9]1[cH:10][c:11]([Cl:16])[c:12]([OH:15])[cH:13][cH:14]1)[CH2:7]2.[CH3:17][c:18]1[cH:19][cH:20][c:21]([S:22]([O:23][CH:28]2[CH2:29][N:30]([C:32](=[O:33])[c:34]3[o:35][c:36](-[c:39]4[cH:40][cH:41][cH:42][cH:43][cH:44]4)[n:37][n:38]3)[CH2:31]2)(=[O:24])=[O:25])[cH:26][cH:27]1>>[CH2:1]1[O:2][CH2:3][C:4]12[CH2:5][N:6]([CH2:8][c:9]1[cH:10][c:11]([Cl:16])[c:12]([O:15][CH:28]3[CH2:29][N:30]([C:32](=[O:33])[c:34]4[o:35][c:36](-[c:39]5[cH:40][cH:41][cH:42][cH:43][cH:44]5)[n:37][n:38]4)[CH2:31]3)[cH:13][cH:14]1)[CH2:7]2Participants
3
Sources & evidence
- ORD record
- ord-35ede66c43ed45279d0173cf85b4933b
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (4/10)
Reaction notes
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