3,4,5-Trifluorobenzyl bromide → HCID 59336127, compound

HRID 2124357Notes

Reaction equation

HRID 2124357 reaction equation
[Br:29][CH2:30][c:31]1[cH:32][c:33]([F:39])[c:34]([F:38])[c:35]([F:37])[cH:36]1.[CH3:1][c:2]1[n:3][c:4]([O:17][CH2:18][C:19](=[O:20])[N:21]([CH:22]2[CH2:23][CH2:24][NH:25][CH2:26][CH2:27]2)[CH3:28])[n:5][c:6]([CH3:16])[c:7]1[NH:8][C:9]([O:10][C:11]([CH3:12])([CH3:13])[CH3:14])=[O:15]>>[CH3:1][c:2]1[n:3][c:4]([O:17][CH2:18][C:19](=[O:20])[N:21]([CH:22]2[CH2:23][CH2:24][N:25]([CH2:30][c:31]3[cH:32][c:33]([F:39])[c:34]([F:38])[c:35]([F:37])[cH:36]3)[CH2:26][CH2:27]2)[CH3:28])[n:5][c:6]([CH3:16])[c:7]1[NH:8][C:9]([O:10][C:11]([CH3:12])([CH3:13])[CH3:14])=[O:15]

Participants

3

Reactant 2

HCID 27770623,4,5-Trifluorobenzyl bromideHCID 59336171Tert-butyl 4,6-dimethyl-2-(2-(methyl(piperidine-4-yl)amino)-2-oxoethoxy)pyrimidine-5-ylcarbamate

Product 1

HCID 59336127HCID 59336127, compound

Sources & evidence

ORD record
ord-d912d27eb03447e3974c5db877468111
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (4/10)

Reaction notes

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