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Potassium Cation → HCID 22320347, compound

HRID 321835
Notes
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Reaction equation

HRID 321835 reaction equation
[C:28](=[O:29])([O-:30])[O-:31].[CH2:22]1[CH2:23][O:24][CH2:25][CH2:26][NH:27]1.[CH3:34][N:35]([CH3:36])[CH:37]=[O:38].[Cl:1][c:2]1[c:3]2[c:4]([n:5][c:6]3[cH:7][cH:8][cH:9][cH:10][c:11]13)[n:12](-[c:16]1[n:17][cH:18][cH:19][cH:20][cH:21]1)[n:13][c:14]2[CH3:15].[K+:32].[K+:33]>>[c:2]1([N:27]2[CH2:22][CH2:23][O:24][CH2:25][CH2:26]2)[c:3]2[c:4]([n:5][c:6]3[cH:7][cH:8][cH:9][cH:10][c:11]13)[n:12](-[c:16]1[n:17][cH:18][cH:19][cH:20][cH:21]1)[n:13][c:14]2[CH3:15]
ParticipantsSources & evidenceReaction notes

Participants

6

Reactant 5

HCID 813Potassium Cation2×HCID 6228DimethylformamideHCID 8083MorpholineHCID 19660Carbonate IonHCID 223201094-Chloro-3-methyl-1-(2-pyridinyl)-1H-pyrazolo[3,4-b]quinoline

Product 1

HCID 22320347HCID 22320347, compound

Sources & evidence

ORD record
ord-eeb311df38714581a358c64af8545b20
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (8/10)
DOI
10.1039/C8SC04228D

Reaction notes

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On this pageParticipantsSources & evidenceReaction notes