Acetyl chloride → HCID 67280153, compound
Reaction equation
[CH2:1]([NH:8][C:9]1[N:14]=[CH:13][C:12]([Br:15])=[CH:11][N:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:16](Cl)(=[O:18])[CH3:17]>>[Br:15][C:12]1[CH:13]=[N:14][C:9]([N:8]([CH2:1][C:2]2[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=2)[C:16](=[O:18])[CH3:17])=[N:10][CH:11]=1Participants
3
Procedure
The subtitle compound was prepared by the method of example 38 step (i) using benzyl-(5-bromo-pyrimidin-2-yl)-amine and acetylchloride, yield 0.21 g.
Sources & evidence
- ORD record
- ord-23b0e5862cd34c3b97cd3a9a0a4e00f1
- Source dataset
- uspto-grants-2012_04
- Patent number
- US08158820B2
Reaction notes
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