Ammonium → HCID 66755623, compound

HRID 289232Notes

Reaction equation

HRID 289232 reaction equation
[Br:21][CH:22]([C:23](=[O:24])[O:25][C:26]([CH3:27])([CH3:28])[CH3:29])[c:30]1[cH:31][cH:32][cH:33][cH:34][cH:35]1.[CH3:43][CH2:44][O:45][C:46](=[O:47])[CH3:48].[Cl-:36].[Cl:1][c:2]1[cH:3][c:4]2[c:5]([n:6]([C:10](=[O:11])[O:12][C:13]([CH3:14])([CH3:15])[CH3:16])[c:7](=[O:9])[nH:8]2)[cH:17][cH:18]1.[H-:19].[NH4+:37].[Na+:20].[O:38]=[CH:39][N:40]([CH3:41])[CH3:42]>>[Cl:1][c:2]1[cH:3][c:4]2[c:5]([n:6]([C:10](=[O:11])[O:12][C:13]([CH3:14])([CH3:15])[CH3:16])[c:7](=[O:9])[n:8]2[CH:22]([C:23](=[O:24])[O:25][C:26]([CH3:27])([CH3:28])[CH3:29])[c:30]2[cH:31][cH:32][cH:33][cH:34][cH:35]2)[cH:17][cH:18]1

Participants

9

Reactant 8

HCID 223AmmoniumHCID 312ChlorideHCID 923Sodium ionHCID 6228DimethylformamideHCID 8857Ethyl AcetateHCID 166653HydrideHCID 10468275tert-Butyl 5-chloro-2-oxo-2,3-dihydrobenzimidazole-1-carboxylateHCID 11000147Tert-butyl 2-bromo-2-phenylacetate

Product 1

HCID 66755623HCID 66755623, compound

Sources & evidence

ORD record
ord-e78fd1e6de004e448827cbeb691771e3
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (8/10)

Reaction notes

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