2-Amino-2-methyl-1-propanol → HCID 178454505, compound
Reaction equation
Br[C:2]1[N:10]=[C:9]([S:11][CH2:12][C:13]2[CH:18]=[CH:17][CH:16]=[C:15]([F:19])[C:14]=2[F:20])[N:8]=[C:7]2[C:3]=1[N:4]=[C:5]([NH:21]C(=O)OCC)[NH:6]2.[NH2:27][C:28]([CH3:32])([CH3:31])[CH2:29][OH:30]>>[NH2:21][C:5]1[NH:6][C:7]2[C:3]([N:4]=1)=[C:2]([NH:27][C:28]([CH3:32])([CH3:31])[CH2:29][OH:30])[N:10]=[C:9]([S:11][CH2:12][C:13]1[CH:18]=[CH:17][CH:16]=[C:15]([F:19])[C:14]=1[F:20])[N:8]=2Participants
3
Procedure
The titled compound was prepared from the product of example 5, step (e) (50 mg) and 2-amino-2-methyl-1-propanol (66 μl) using the method of example 5, step (f) and purified by preparative HPLC to yield a white solid.
Workup
- custompurified by preparative HPLC
- customto yield a white solid
Sources & evidence
- ORD record
- ord-f4f7eacc037d42829aea207659d2abe2
- Source dataset
- uspto-grants-2005_10
- Patent number
- US06958344B2
Reaction notes
Loading…