Pyridine → HCID 67255836, compound

HRID 2336181Notes

Reaction equation

HRID 2336181 reaction equation
[CH2:40]1[O:41][CH2:42][CH2:43][CH2:44]1.[Cl:1][c:2]1[cH:3][c:4]([NH2:20])[cH:5][c:6]([Cl:19])[c:7]1[S:8][c:9]1[cH:10][c:11]2[cH:12][cH:13][cH:14][cH:15][c:16]2[cH:17][cH:18]1.[Cl:27][c:28]1[n:29][c:30]2[s:31][cH:32][cH:33][n:34]2[c:35]1[S:36](=[O:37])(=[O:38])[Cl:39].[cH:21]1[cH:22][cH:23][n:24][cH:25][cH:26]1>>[Cl:1][c:2]1[cH:3][c:4]([NH:20][S:36]([c:35]2[c:28]([Cl:27])[n:29][c:30]3[s:31][cH:32][cH:33][n:34]32)(=[O:37])=[O:38])[cH:5][c:6]([Cl:19])[c:7]1[S:8][c:9]1[cH:10][c:11]2[cH:12][cH:13][cH:14][cH:15][c:16]2[cH:17][cH:18]1

Participants

5

Reactant 4

HCID 1049PyridineHCID 8028TetrahydrofuranHCID 27997176-Chloroimidazo(2,1-b)(1,3)thiazole-5-sulfonyl chlorideHCID 221488343,5-Dichloro-4-(napthalen-2-ylsulfanyl)-phenylamine

Product 1

HCID 67255836HCID 67255836, compound

Sources & evidence

ORD record
ord-051b008c646246be98f095aefb97ed10
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (10/10)

Reaction notes

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