Dimethyl Sulfone → HCID 69809288, compound
Reaction equation
[CH3:1][S:2]([N:5]1[CH2:10][CH2:9][CH2:8][C@H:7]([NH:11][C:12]2[C:17]([C:18]3[N:19]=[C:20]4[CH:26]=[CH:25][N:24](COCC[Si](C)(C)C)[C:21]4=[N:22][CH:23]=3)=[CH:16][N:15]=[C:14](S(C)(=O)=O)[N:13]=2)[CH2:6]1)(=[O:4])=[O:3].[NH:39]1[CH2:44][CH2:43][CH:42]([CH2:45][C:46]([OH:48])=[O:47])[CH2:41][CH2:40]1.CS(C)(=O)=O>O1CCOCC1>[CH3:1][S:2]([N:5]1[CH2:10][CH2:9][CH2:8][C@H:7]([NH:11][C:12]2[C:17]([C:18]3[N:19]=[C:20]4[CH:26]=[CH:25][NH:24][C:21]4=[N:22][CH:23]=3)=[CH:16][N:15]=[C:14]([N:39]3[CH2:44][CH2:43][CH:42]([CH2:45][C:46]([OH:48])=[O:47])[CH2:41][CH2:40]3)[N:13]=2)[CH2:6]1)(=[O:4])=[O:3]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
In a dioxane solution of ((S)-1-methanesulfonyl-piperidin-3-yl)-{2-methanesulfonyl-5-[5-(2-trimethylsilanyl-ethoxymethyl)-5H-pyrrolo[2,3-b]pyrazin-2-yl]-pyrimidin-4-yl}-amine derived from Example 84, step 1, Piperidin-4-yl-acetic acid was used to displace the methylsulfone similar to examples above and the de-protection step was similar to step 5, Example 76, to give {1-[4-((S)-1-Methanesulfonyl-piperidin-3-ylamino)-5-(5H-pyrrolo[2,3-b]pyrazin-2-yl)-pyrimidin-2-yl]-piperidin-4-yl}-acetic acid. MS: (ES+): 515
Sources & evidence
- ORD record
- ord-9c2f8f9af4e44932ad2c5f25382ee301
- Source dataset
- uspto-grants-2013_12
- Patent number
- US08618103B2
Reaction notes
Loading…