Benzoyl chloride → 18-Benzoyloxy-14-tert-butoxycarbonylamino-4-cyclopropylsulfonylaminocarbonyl-2,15-dioxo-3,16-diaza-12-oxatricyclo-[14.3.0.04,6]-nonadec-7-ene

HRID 197139

Reaction equation

HRID 197139 reaction equation
[C:40]([c:41]1[cH:42][cH:43][cH:44][cH:45][cH:46]1)(=[O:47])[Cl:48].[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:40]([c:41]1[cH:42][cH:43][cH:44][cH:45][cH:46]1)=[O:47]

Participants

3

Reactant 2

HCID 7412Benzoyl chlorideHCID 7226012718-Hydroxy-14-tert-butoxycarbonylamino-4-cyclopropylsulfonylaminocarbonyl-2,15-dioxo-3,16-diaza-12-oxatricyclo[14.3.0.04,6]-nonadec-7-ene

Product 1

HCID 7244537418-Benzoyloxy-14-tert-butoxycarbonylamino-4-cyclopropylsulfonylaminocarbonyl-2,15-dioxo-3,16-diaza-12-oxatricyclo-[14.3.0.04,6]-nonadec-7-ene

Sources & evidence

ORD record
ord-9656992ad39946538440be92a78a003e
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (6/10)

Linked notes

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