Dimethylsulphamoyl chloride → Hydrochloric Acid

HRID 2323700Notes

Reaction equation

HRID 2323700 reaction equation
[CH3:1][c:2]1[n:3][cH:4][cH:5][cH:6][c:7]1[O:8][c:9]1[c:10]([NH:22][c:23]2[n:24][c:25]([CH:28]3[CH2:29][CH2:30][NH:31][CH2:32][CH2:33]3)[n:26][s:27]2)[n:11][cH:12][c:13]([S:15][c:16]2[n:17][cH:18][cH:19][cH:20][cH:21]2)[cH:14]1.[CH3:34][N:35]([S:36](=[O:37])(=[O:38])[Cl:39])[CH3:40]>>[CH3:1][c:2]1[n:3][cH:4][cH:5][cH:6][c:7]1[O:8][c:9]1[c:10]([NH:22][c:23]2[n:24][c:25]([CH:28]3[CH2:29][CH2:30][N:31]([S:36]([N:35]([CH3:34])[CH3:40])(=[O:37])=[O:38])[CH2:32][CH2:33]3)[n:26][s:27]2)[n:11][cH:12][c:13]([S:15][c:16]2[n:17][cH:18][cH:19][cH:20][cH:21]2)[cH:14]1.[ClH:39]

Participants

4

Reactant 2

HCID 83372Dimethylsulphamoyl chlorideHCID 67487355N-(3-(2-methylpyridin-3-yloxy)-5-(pyridin-2-ylthio)pyridin-2-yl)-3-(piperidin-4-yl)-1,2,4-thiadiazol-5-amine

Product 2

HCID 313Hydrochloric AcidHCID 59291622HCID 59291622, compound

Sources & evidence

ORD record
ord-1a13addcb79e4cc595f13edb7292a7e0
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (10/10)

Reaction notes

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