Bromide ion → N-(2-(5-bromopyridin-3-yl)propan-2-yl)ethanesulfonamide

Reaction equation

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

Participants

Reactant 7

HCID 259Bromide ion

HCID 1140Toluene

HCID 73702Ethanesulfonamide

HCID 114942Titanium cation (4+)

HCID 8204233-Acetyl-5-bromopyridine

HCID 3260420Isopropanolate4×

HCID 178477777HCID 178477777, compound

Product 1

Sources & evidence

ORD record: ord-5f5b7aab59a94cb19e570bf833dc48a1
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (10/10)
DOI: 10.1039/C8SC04228D

Reaction notes

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