4-Phenoxybenzoyl chloride → 18-(4-Phenoxybenzoyloxy)-14-tert-butoxycarbonylamino-4-cyclopropylsulfonylaminocarbonyl-2,15-dioxo-3,16-diaza-12-oxatricyclo-[14.3.0.04,6]-nonadec-7-ene
Reaction equation
[O:40]([c:41]1[cH:42][cH:43][cH:44][cH:45][cH:46]1)[c:47]1[cH:48][cH:49][c:50]([C:51](=[O:52])[Cl:53])[cH:54][cH:55]1.[OH:1][CH:2]1[CH2:3][N:4]2[C:5](=[O:39])[CH:6]([NH:31][C:32](=[O:33])[O:34][C:35]([CH3:36])([CH3:37])[CH3:38])[CH2:7][O:8][CH2:9][CH2:10][CH2:11][CH:12]=[CH:13][CH:14]3[CH2:15][C:16]3([C:22](=[O:23])[NH:24][S:25](=[O:26])(=[O:27])[CH:28]3[CH2:29][CH2:30]3)[NH:17][C:18](=[O:21])[CH:19]2[CH2:20]1>>[O:1]([CH:2]1[CH2:3][N:4]2[C:5](=[O:39])[CH:6]([NH:31][C:32](=[O:33])[O:34][C:35]([CH3:36])([CH3:37])[CH3:38])[CH2:7][O:8][CH2:9][CH2:10][CH2:11][CH:12]=[CH:13][CH:14]3[CH2:15][C:16]3([C:22](=[O:23])[NH:24][S:25](=[O:26])(=[O:27])[CH:28]3[CH2:29][CH2:30]3)[NH:17][C:18](=[O:21])[CH:19]2[CH2:20]1)[C:51]([c:50]1[cH:49][cH:48][c:47]([O:40][c:41]2[cH:42][cH:43][cH:44][cH:45][cH:46]2)[cH:55][cH:54]1)=[O:52]Participants
3
Reactant 2
Product 1
Sources & evidence
- ORD record
- ord-b37c841083f64fa587eb73ad42f637cc
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (4/10)
Reaction notes
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