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Dimethyl Sulfoxide → HCID 178489346, compound

HRID 2331102
Notes
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Reaction equation

HRID 2331102 reaction equation
[CH2:11]1[N:12]2[CH2:13][CH2:14][N:15]([CH2:16][CH2:17]2)[CH2:18]1.[CH3:21][O:22][c:23]1[c:24](-[c:29]2[n:30][c:31]3[c:32]([CH3:41])[cH:33][cH:34][cH:35][c:36]3[cH:37][c:38]2[CH2:39][OH:40])[cH:25][cH:26][cH:27][cH:28]1.[CH3:42][S:43]([CH3:44])=[O:45].[Cl:1][c:2]1[c:3]2[nH:4][cH:5][n:6][c:7]2[n:8][cH:9][n:10]1.[H-:19].[Na+:20]>>[c:2]1([O:40][CH2:39][c:38]2[c:29](-[c:24]3[c:23]([O:22][CH3:21])[cH:28][cH:27][cH:26][cH:25]3)[n:30][c:31]3[c:32]([CH3:41])[cH:33][cH:34][cH:35][c:36]3[cH:37]2)[c:3]2[n:4][cH:5][nH:6][c:7]2[n:8][cH:9][n:10]1
ParticipantsSources & evidenceReaction notes

Participants

7

Reactant 6

HCID 679Dimethyl SulfoxideHCID 923Sodium IonHCID 9237DabcoHCID 166653HydrideHCID 53592776-ChloropurineHCID 57707787(2-(2-Methoxyphenyl)-8-methylquinolin-3-yl)methanol

Product 1

HCID 178489346
HCID 178489346, compound

Sources & evidence

ORD record
ord-2ba7916c0146458ea36046574b1ac161
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (10/10)
DOI
10.1039/C8SC04228D

Reaction notes

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On this pageParticipantsSources & evidenceReaction notes