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Potassium Cation → 4-(1H-indol-5-yloxy)-5-(3,4-dimethoxyphenyl)nicotinonitrile

HRID 827540
Notes
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Reaction equation

HRID 827540 reaction equation
[CH3:36][C:37]#[N:38].[Cl:1][c:2]1[c:3](-[c:10]2[cH:11][c:12]([O:18][CH3:19])[c:13]([O:16][CH3:17])[cH:14][cH:15]2)[cH:4][n:5][cH:6][c:7]1[C:8]#[N:9].[K+:30].[K+:31].[O-:32][C:33]([O-:34])=[O:35].[OH2:39].[OH:20][c:21]1[cH:22][c:23]2[cH:24][cH:25][nH:26][c:27]2[cH:28][cH:29]1>>[c:2]1([O:20][c:21]2[cH:22][c:23]3[cH:24][cH:25][nH:26][c:27]3[cH:28][cH:29]2)[c:3](-[c:10]2[cH:11][c:12]([O:18][CH3:19])[c:13]([O:16][CH3:17])[cH:14][cH:15]2)[cH:4][n:5][cH:6][c:7]1[C:8]#[N:9]
ParticipantsSources & evidenceReaction notes

Participants

7

Reactant 6

HCID 813Potassium Cation2×HCID 962WaterHCID 6342AcetonitrileHCID 160545-HydroxyindoleHCID 19660Carbonate IonHCID 251297854-Chloro-5-(3,4-dimethoxyphenyl)nicotinonitrile

Product 1

Sources & evidence

ORD record
ord-ba96ac3fd2864de69d468c1d3305776a
Source dataset
Test data from https://doi.org/10.1039/C8SC04228D
DOI
10.1039/C8SC04228D

Reaction notes

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On this pageParticipantsSources & evidenceReaction notes
HCID 44573872
4-(1H-indol-5-yloxy)-5-(3,4-dimethoxyphenyl)nicotinonitrile