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Potassium Cation → HCID 59242107, compound

HRID 1546858
Notes
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Reaction equation

HRID 1546858 reaction equation
[Br:27][CH2:28][C:29](=[O:30])[O:31][CH3:32].[CH3:38][CH2:39][O:40][C:41]([CH3:42])=[O:43].[K+:21].[K+:22].[O-:23][C:24]([O-:25])=[O:26].[O:33]=[CH:34][N:35]([CH3:36])[CH3:37].[OH:1][c:2]1[cH:3][cH:4][c:5]([N:8]([CH3:9])[c:10]2[n:11][c:12]([CH3:20])[n:13][c:14]3[cH:15][cH:16][cH:17][cH:18][c:19]23)[cH:6][cH:7]1>>[O:1]([c:2]1[cH:3][cH:4][c:5]([N:8]([CH3:9])[c:10]2[n:11][c:12]([CH3:20])[n:13][c:14]3[cH:15][cH:16][cH:17][cH:18][c:19]23)[cH:6][cH:7]1)[CH2:28][C:29](=[O:30])[O:31][CH3:32]
ParticipantsSources & evidenceReaction notes

Participants

7

Reactant 6

HCID 813Potassium Cation2×HCID 6228DimethylformamideHCID 8857Ethyl AcetateHCID 19660Carbonate IonHCID 60984Methyl bromoacetateHCID 114710894-(methyl(2-methylquinazolin-4-yl)amino)phenol

Product 1

On this pageParticipantsSources & evidenceReaction notes
HCID 59242107
HCID 59242107, compound

Sources & evidence

ORD record
ord-4222aebfd12545c5b5c58bdca9db28fc
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (1/10)
DOI
10.1039/C8SC04228D

Reaction notes

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