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Potassium Cation → Methyl 3-[5-(quinolin-2-ylmethoxy)indol-2-yl]-2,2-dimethylpropanoate

HRID 1152697
Notes
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Reaction equation

HRID 1152697 reaction equation
[Br:19][CH2:20][c:21]1[n:22][c:23]2[cH:24][cH:25][cH:26][cH:27][c:28]2[cH:29][cH:30]1.[K+:31].[K+:32].[O-:33][C:34]([O-:35])=[O:36].[O:37]=[CH:38][N:39]([CH3:40])[CH3:41].[OH:1][c:2]1[cH:3][c:4]2[cH:5][c:6]([CH2:11][C:12]([C:13](=[O:14])[O:15][CH3:16])([CH3:17])[CH3:18])[nH:7][c:8]2[cH:9][cH:10]1>>[O:1]([c:2]1[cH:3][c:4]2[cH:5][c:6]([CH2:11][C:12]([C:13](=[O:14])[O:15][CH3:16])([CH3:17])[CH3:18])[nH:7][c:8]2[cH:9][cH:10]1)[CH2:20][c:21]1[n:22][c:23]2[cH:24][cH:25][cH:26][cH:27][c:28]2[cH:29][cH:30]1
ParticipantsSources & evidenceReaction notes

Participants

6

Reactant 5

HCID 813Potassium Cation2×HCID 6228DimethylformamideHCID 19660Carbonate IonHCID 124174182-(Bromomethyl)quinolineHCID 18947616Methyl 3-[5-hydroxyindol-2-yl]-2,2-dimethylpropanoate

Product 1

HCID 18947552Methyl 3-[5-(quinolin-2-ylmethoxy)indol-2-yl]-2,2-dimethylpropanoate

Sources & evidence

ORD record
ord-385f7c7294bf4b4fae2b45b58a9beb32
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (7/10)
DOI
10.1039/C8SC04228D

Reaction notes

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On this pageParticipantsSources & evidenceReaction notes