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Ammonium → (6-Bromo-naphthalen-2-yl)-(6,7-dimethoxy-quinolin-4-yl)-methanol

HRID 173842
Notes
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Reaction equation

HRID 173842 reaction equation
[Br:23][Mg:24][c:25]1[cH:26][cH:27][cH:28][cH:29][cH:30]1.[Br:31][c:32]1[cH:33][c:34]2[cH:35][cH:36][c:37]([CH:42]=[O:43])[cH:38][c:39]2[cH:40][cH:41]1.[CH2:46]1[O:47][CH2:48][CH2:49][CH2:50]1.[Cl-:44].[NH4+:45].[c:1]1([S:2](=[O:3])[c:9]2[cH:10][cH:11][n:12][c:13]3[cH:14][c:15]([O:21][CH3:22])[c:16]([O:19][CH3:20])[cH:17][c:18]23)[cH:4][cH:5][cH:6][cH:7][cH:8]1>>[c:9]1([CH:42]([c:37]2[cH:36][cH:35][c:34]3[cH:33][c:32]([Br:31])[cH:41][cH:40][c:39]3[cH:38]2)[OH:43])[cH:10][cH:11][n:12][c:13]2[cH:14][c:15]([O:21][CH3:22])[c:16]([O:19][CH3:20])[cH:17][c:18]12
ParticipantsSources & evidenceReaction notes

Participants

7

Reactant 6

HCID 223AmmoniumHCID 312ChlorideHCID 8028TetrahydrofuranHCID 134770296-Bromonaphthalene-2-carbaldehydeHCID 675205384-Benzenesulfinyl-6,7-dimethoxy-quinolineHCID 178418255HCID 178418255, compound

Product 1

HCID 67520432
(6-Bromo-naphthalen-2-yl)-(6,7-dimethoxy-quinolin-4-yl)-methanol

Sources & evidence

ORD record
ord-86c3d3f77d784e0ea831a27b96ffeb4d
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (9/10)
DOI
10.1039/C8SC04228D

Reaction notes

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On this pageParticipantsSources & evidenceReaction notes