Dichloromethane → HCID 59613513, compound

HRID 302997Notes

Reaction equation

[C:1](#[N:2])[c:3]1[n:4][cH:5][c:6]([NH:9][c:10]2[n:11][cH:12][c:13](-[c:31]3[n:32][c:33]([CH3:36])[n:34][o:35]3)[c:14]([NH:16][CH2:17][CH:18]3[CH2:19][CH2:20][N:21]([C:24]([O:25][C:26]([CH3:27])([CH3:28])[CH3:29])=[O:30])[CH2:22][CH2:23]3)[cH:15]2)[n:7][cH:8]1.[Cl:44][CH2:45][Cl:46].[OH:37][C:38]([C:39]([F:40])([F:41])[F:42])=[O:43]>>[C:1](#[N:2])[c:3]1[n:4][cH:5][c:6]([NH:9][c:10]2[n:11][cH:12][c:13](-[c:31]3[n:32][c:33]([CH3:36])[n:34][o:35]3)[c:14]([NH:16][CH2:17][CH:18]3[CH2:19][CH2:20][NH:21][CH2:22][CH2:23]3)[cH:15]2)[n:7][cH:8]1

Participants

Reactant 3

HCID 6344Dichloromethane

HCID 6422Trifluoroacetic acid

HCID 59613367tert-Butyl 4-((2-(5-cyanopyrazin-2-ylamino)-5-(3-methyl-1,2,4-oxadiazol-5-yl)pyridin-4-ylamino)methyl)piperidine-1-carboxylate

Product 1

HCID 59613513HCID 59613513, compound

Sources & evidence

ORD record: ord-99846fd7c04e4228926cbb58e8882e72
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (8/10)
DOI: 10.1039/C8SC04228D

Reaction notes

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