1-(Bromomethyl)-4-ethylbenzene → 2-Bromo-4-{2-[(4-ethylbenzyl)(5-ethylpyrimidin-2-yl)amino]ethyl}phenol
Reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([CH2:10][CH2:11][NH:12][C:13]2[N:18]=[CH:17][C:16]([CH2:19][CH3:20])=[CH:15][N:14]=2)[CH:5]=[CH:6][C:7]=1[O:8]C.[CH2:21]([C:23]1[CH:30]=[CH:29][C:26]([CH2:27]Br)=[CH:25][CH:24]=1)[CH3:22]>>[Br:1][C:2]1[CH:3]=[C:4]([CH2:10][CH2:11][N:12]([CH2:27][C:26]2[CH:29]=[CH:30][C:23]([CH2:21][CH3:22])=[CH:24][CH:25]=2)[C:13]2[N:18]=[CH:17][C:16]([CH2:19][CH3:20])=[CH:15][N:14]=2)[CH:5]=[CH:6][C:7]=1[OH:8]Participants
3
Procedure
Similarly prepared from N-[2-(3-bromo-4-methoxyphenyl)ethyl]-5-ethylpyrimidin-2-amine and 4-ethyl benzyl bromide.
Sources & evidence
- ORD record
- ord-b2b25635311c40e698d2e4ab04911893
- Source dataset
- uspto-grants-2008_01
- Patent number
- US07319104B2
Reaction notes
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