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Ammonium → 5-Bromo-2-(4-methanesulfonylbenzyloxy)pyridine

HRID 107876
Notes
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Reaction equation

HRID 107876 reaction equation
[Br:1][c:2]1[n:3][cH:4][c:5]([Br:8])[cH:6][cH:7]1.[CH3:21][C:22]([CH3:23])([O-:24])[CH3:25].[CH3:9][S:10](=[O:11])(=[O:12])[c:13]1[cH:14][cH:15][c:16]([CH2:17][OH:18])[cH:19][cH:20]1.[Cl-:27].[K+:26].[NH4+:28].[O:29]1[CH2:30][CH2:31][CH2:32][CH2:33]1>>[c:2]1([O:18][CH2:17][c:16]2[cH:15][cH:14][c:13]([S:10]([CH3:9])(=[O:11])=[O:12])[cH:20][cH:19]2)[n:3][cH:4][c:5]([Br:8])[cH:6][cH:7]1
ParticipantsSources & evidenceReaction notes

Participants

8

Reactant 7

HCID 223AmmoniumHCID 312ChlorideHCID 813Potassium CationHCID 8028TetrahydrofuranHCID 693532,5-DibromopyridineHCID 3801026(4-Methanesulfonylphenyl)methanolHCID 45749132-Methylpropan-2-olate

Product 1

Sources & evidence

ORD record
ord-2811a892d80a4d2f923f3bd1980b13fd
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (2/10)
DOI
10.1039/C8SC04228D

Reaction notes

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On this pageParticipantsSources & evidenceReaction notes
HCID 67083256
5-Bromo-2-(4-methanesulfonylbenzyloxy)pyridine