3,5-Dimethylpyridine → HCID 12021108, compound

HRID 1567163Notes

Reaction equation

HRID 1567163 reaction equation
[Br:1][c:2]1[cH:3][c:4]2[n:5]3[c:6]4[c:7]([cH:8][c:9]([OH:16])[cH:10][c:11]4[s:12][c:13]2[cH:14][cH:15]1)[c:17](=[O:27])[c:18]([CH2:20][c:21]1[cH:22][n:23][cH:24][cH:25][cH:26]1)[cH:19]3.[CH3:37][c:38]1[cH:39][n:40][cH:41][c:42]([CH3:43])[cH:44]1.[Cl:28][CH2:29][c:30]1[cH:31][n:32][cH:33][c:34]([CH3:36])[cH:35]1>>[Br:1][c:2]1[cH:3][c:4]2[n:5]3[c:6]4[c:7]([cH:8][c:9]([O:16][CH2:29][c:30]5[cH:31][n:32][cH:33][c:34]([CH3:36])[cH:35]5)[cH:10][c:11]4[s:12][c:13]2[cH:14][cH:15]1)[c:17](=[O:27])[c:18]([CH2:20][c:21]1[cH:22][n:23][cH:24][cH:25][cH:26]1)[cH:19]3

Participants

4

Reactant 3

HCID 115653,5-DimethylpyridineHCID 119627823-(CHLOROMETHYL)-5-METHYLPYRIDINEHCID 1202110510-bromo-5-hydroxy-2-(3-pyridylmethyl)-3H-pyrido[3,2,1-kl]phenothiazin-3-one

Product 1

HCID 12021108HCID 12021108, compound

Sources & evidence

ORD record
ord-99db911d0aee441fb3b81370ec80ee55
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (1/10)

Reaction notes

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