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Dimethyl Sulfoxide → 3-(7-Chloroquinolin-4-yloxy)-5,6,5'-trimethyl-[2,2']-bipyridine

HRID 2124855
Notes
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Reaction equation

HRID 2124855 reaction equation
[C:33](=[O:34])([O-:35])[O-:36].[CH3:1][S:2](=[O:3])[CH3:4].[CH3:5][c:6]1[cH:7][c:8]([OH:20])[c:9](-[c:13]2[n:14][cH:15][c:16]([CH3:19])[cH:17][cH:18]2)[n:10][c:11]1[CH3:12].[Cl:21][c:22]1[cH:23][cH:24][n:25][c:26]2[cH:27][c:28]([Cl:32])[cH:29][cH:30][c:31]12.[Cs+:37].[Cs+:38].[OH2:39]>>[CH3:5][c:6]1[cH:7][c:8]([O:20][c:22]2[cH:23][cH:24][n:25][c:26]3[cH:27][c:28]([Cl:32])[cH:29][cH:30][c:31]23)[c:9](-[c:13]2[n:14][cH:15][c:16]([CH3:19])[cH:17][cH:18]2)[n:10][c:11]1[CH3:12]
ParticipantsSources & evidenceReaction notes

Participants

7

Reactant 6

HCID 679Dimethyl SulfoxideHCID 962WaterHCID 68664,7-DichloroquinolineHCID 19660Carbonate IonHCID 104967Cesium cation2×HCID 1363851085,6,5'-Trimethyl-[2,2']bipyridin-3-ol

Product 1

On this pageParticipantsSources & evidenceReaction notes
HCID 57756599
3-(7-Chloroquinolin-4-yloxy)-5,6,5'-trimethyl-[2,2']-bipyridine

Sources & evidence

ORD record
ord-126fedaf808949889ef1cbc12493d59f
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (4/10)
DOI
10.1039/C8SC04228D

Reaction notes

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