Hydrochloric Acid → HCID 11610950, compound
Reaction equation
[CH3:1][S:2]([C:5]1[CH:10]=[CH:9][C:8](B(O)O)=[CH:7][CH:6]=1)(=[O:4])=[O:3].Br[C:15]1[CH:20]=[CH:19][C:18]([C:21]2[O:22][CH:23]=[C:24]([CH2:26][N:27]3[CH2:31][CH2:30][CH2:29][CH:28]3[CH3:32])[N:25]=2)=[CH:17][CH:16]=1.Cl>>[CH3:1][S:2]([C:5]1[CH:10]=[CH:9][C:8]([C:15]2[CH:20]=[CH:19][C:18]([C:21]3[O:22][CH:23]=[C:24]([CH2:26][N:27]4[CH2:31][CH2:30][CH2:29][CH:28]4[CH3:32])[N:25]=3)=[CH:17][CH:16]=2)=[CH:7][CH:6]=1)(=[O:4])=[O:3]Participants
4
Procedure
The titled compound is prepared substantially in accordance with the procedure of Example 4 using 4-methylsulfonylphenylboronic acid and (+/−)-2-(4-Bromo-phenyl)-4-(2-methyl-pyrrolidin-1-ylmethyl)-oxazole; hydrochloride (See Example 5). MS (m/e) 397.1 (M+1)
Sources & evidence
- ORD record
- ord-871d3a5ff7984bc98290eb77e72e43ec
- Source dataset