Pyridine → HCID 44125258, compound

HRID 2128317Notes

Reaction equation

HRID 2128317 reaction equation
[Cl:22][c:23]1[c:24]([S:30](=[O:31])(=[O:32])[Cl:33])[c:25]([CH3:29])[cH:26][cH:27][cH:28]1.[NH2:1][c:2]1[cH:3][c:4](-[c:9]2[cH:10][cH:11][c:12]3[n:13]([n:14]2)[cH:15][c:16]([NH:18][C:19]([CH3:20])=[O:21])[n:17]3)[cH:5][n:6][c:7]1[Cl:8].[cH:34]1[cH:35][cH:36][n:37][cH:38][cH:39]1>>[NH:1]([c:2]1[cH:3][c:4](-[c:9]2[cH:10][cH:11][c:12]3[n:13]([n:14]2)[cH:15][c:16]([NH:18][C:19]([CH3:20])=[O:21])[n:17]3)[cH:5][n:6][c:7]1[Cl:8])[S:30]([c:24]1[c:23]([Cl:22])[cH:28][cH:27][cH:26][c:25]1[CH3:29])(=[O:31])=[O:32]

Participants

4

Reactant 3

HCID 1049PyridineHCID 157253702-Chloro-6-methylbenzene-1-sulfonyl chlorideHCID 57749424N-(6-(5-amino-6-chloropyridin-3-yl)imidazo[1,2-b]pyridazin-2-yl)acetamide

Product 1

HCID 44125258HCID 44125258, compound

Sources & evidence

ORD record
ord-11b10b31dbdd45c8b337cd3fd7af83db
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (4/10)

Reaction notes

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