Dichloromethane → (6-(6-Chloro-2-methyl-3-oxo-2,3-dihydropyridazin-4-ylamino)pyridin-3-yl)methyl methanesulfonate

HRID 2133906Notes

Reaction equation

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

Participants

Reactant 4

HCID 6344Dichloromethane

HCID 31297Methanesulfonyl chloride

HCID 81531Diisopropylethylamine

HCID 580437626-Chloro-4-(5-(hydroxymethyl)pyridin-2-ylamino)-2-methylpyridazin-3(2H)-one

Product 1

HCID 58043865(6-(6-Chloro-2-methyl-3-oxo-2,3-dihydropyridazin-4-ylamino)pyridin-3-yl)methyl methanesulfonate

Sources & evidence

ORD record: ord-ea508a1f21bd434389ab31b2d9a757fd
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (4/10)
DOI: 10.1039/C8SC04228D

Reaction notes

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