5-Bromo-2,4-dichloropyrimidine → HCID 123674961, compound

HRID 1121131Notes

Reaction equation

HRID 1121131 reaction equation
[Br:15][c:16]1[c:17]([Cl:23])[n:18][c:19]([Cl:22])[n:20][cH:21]1.[Br:24][c:25]1[c:26]([NH:27][CH:28]([CH:29]([CH3:30])[CH3:31])[CH2:32][NH:33][C:34](=[O:35])[O:36][C:37]([CH3:38])([CH3:39])[CH3:40])[n:41][c:42]([Cl:43])[n:44][cH:45]1.[NH2:1][CH:2]1[CH:3]([NH:7][C:8]([O:9][C:10]([CH3:11])([CH3:12])[CH3:13])=[O:14])[CH2:4][CH2:5][CH2:6]1>>[NH:1]([CH:2]1[CH:3]([NH:7][C:8]([O:9][C:10]([CH3:11])([CH3:12])[CH3:13])=[O:14])[CH2:4][CH2:5][CH2:6]1)[c:17]1[c:16]([Br:15])[cH:21][n:20][c:19]([Cl:22])[n:18]1

Participants

4

Reactant 3

HCID 2899735-Bromo-2,4-dichloropyrimidineHCID 22667934tert-Butyl (2-aminocyclopentyl)carbamateHCID 86695593tert-butyl N-[2-[(5-bromo-2-chloro-pyrimidin-4-yl)amino]-3-methyl-butyl]carbamate

Product 1

HCID 123674961HCID 123674961, compound

Sources & evidence

ORD record
ord-7d7fb68b2b2d4d89aadcac3b288de417
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (7/10)

Reaction notes

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