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Ammonium → 8-(6-Aminohexyloxy)-4-(3,5-dichloropyridin-4-ylamino)-7-methoxyquinolin-2(1H)-one

HRID 204341
Notes
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Reaction equation

HRID 204341 reaction equation
[Cl:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][O:8][c:9]1[c:10]([O:29][CH3:30])[cH:11][cH:12][c:13]2[c:14]([NH:20][c:21]3[c:22]([Cl:28])[cH:23][n:24][cH:25][c:26]3[Cl:27])[cH:15][c:16](=[O:19])[nH:17][c:18]12.[NH4+:31].[OH-:32]>>[CH2:2]([CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][O:8][c:9]1[c:10]([O:29][CH3:30])[cH:11][cH:12][c:13]2[c:14]([NH:20][c:21]3[c:22]([Cl:28])[cH:23][n:24][cH:25][c:26]3[Cl:27])[cH:15][c:16](=[O:19])[nH:17][c:18]12)[NH2:31]
ParticipantsSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 223AmmoniumHCID 961HydroxideHCID 592681178-(6-chlorohexyloxy)-4-(3,5-dichloropyridin-4-ylamino)-7-methoxyquinolin-2(1H)-one

Product 1

HCID 533464738-(6-Aminohexyloxy)-4-(3,5-dichloropyridin-4-ylamino)-7-methoxyquinolin-2(1H)-one

Sources & evidence

ORD record
ord-a4caa21b29b74caa854c41f54e6b0f1e
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (6/10)
DOI
10.1039/C8SC04228D

Reaction notes

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