Bromide ion → HCID 59578412, compound

HRID 685878Notes

Reaction equation

[Br-:16].[Br:1][c:2]1[cH:3][c:4]([CH:8]=[O:9])[cH:5][n:6][cH:7]1.[CH2:10]([CH3:11])[S:12](=[O:13])(=[O:14])[NH2:15].[CH3:25][c:26]1[cH:27][cH:28][cH:29][cH:30][cH:31]1.[CH3:32][CH:33]([CH3:34])[O-:35].[CH3:37][CH:38]([CH3:39])[O-:40].[CH3:41][CH:42]([CH3:43])[O-:44].[CH3:45][CH:46]([CH3:47])[O-:48].[F:17][c:18]1[cH:19][cH:20][c:21]([Mg+:24])[cH:22][cH:23]1.[Ti+4:36]>>[Br:1][c:2]1[cH:3][c:4]([CH:8]([NH:15][S:12]([CH2:10][CH3:11])(=[O:13])=[O:14])[c:21]2[cH:20][cH:19][c:18]([F:17])[cH:23][cH:22]2)[cH:5][n:6][cH:7]1

Participants

Reactant 7

HCID 259Bromide ion

HCID 1140Toluene

HCID 73702Ethanesulfonamide

HCID 114942Titanium cation (4+)

HCID 27847345-Bromo-3-pyridinecarboxaldehyde

HCID 3260420Isopropanolate4×

HCID 178505839HCID 178505839, compound

Product 1

HCID 59578412HCID 59578412, compound

Sources & evidence

ORD record: ord-23fabead532d490896392df257289857
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (3/10)
DOI: 10.1039/C8SC04228D

Reaction notes

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