Pyridine → HCID 57954440, compound

Reaction equation

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

Participants

Reactant 4

HCID 1049Pyridine

HCID 6344Dichloromethane

HCID 815143,3-Dimethylbutanoyl chloride

HCID 27611434-(5-Piperidin-4-yl-1,2,4-oxadiazol-3-yl)pyridine

Product 1

HCID 57954440HCID 57954440, compound

Sources & evidence

ORD record: ord-931d509f10a04145b63cd5a4cd2f2383
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (10/10)
DOI: 10.1039/C8SC04228D

Reaction notes

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