Hydrochloric Acid → 2-(1-Tert-butoxycarbonyl-indol-3-yl)-2-oxo-ethylisocyanate
Reaction equation
[CH3:60][CH2:61][O:62][C:63](=[O:64])[CH3:65].[CH3:66][CH2:67][O:68][CH2:69][CH3:70].[Cl:44][C:45](=[O:46])[Cl:47].[Cl:48][C:49]([Cl:50])([O:51][C:52](=[O:53])[O:54][C:55]([Cl:56])([Cl:57])[Cl:58])[Cl:59].[Cl:71][CH2:72][Cl:73].[ClH:23].[H-:21].[NH2:1][CH2:2][C:3](=[O:4])[c:5]1[cH:6][n:7]([C:14](=[O:15])[O:16][C:17]([CH3:18])([CH3:19])[CH3:20])[c:8]2[cH:9][cH:10][cH:11][cH:12][c:13]12.[NH2:24][CH2:25][C:26](=[O:27])[c:28]1[c:29]2[c:30]([cH:31][cH:32][cH:33][cH:34]2)[n:35]([C:36]([O:37][C:38]([CH3:39])([CH3:40])[CH3:41])=[O:42])[cH:43]1.[Na+:22].[cH:74]1[cH:75][cH:76][n:77][cH:78][cH:79]1>>[N:1]([CH2:2][C:3](=[O:4])[c:5]1[cH:6][n:7]([C:14](=[O:15])[O:16][C:17]([CH3:18])([CH3:19])[CH3:20])[c:8]2[cH:9][cH:10][cH:11][cH:12][c:13]12)=[C:26]=[O:27]Participants
11
Reactant 10
Product 1
Sources & evidence
- ORD record
- ord-2698d1cec28f4f68ba4e507bfb556e0e
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (7/10)
Reaction notes
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