Dimethyl Sulfone → HCID 69810538, compound

HRID 1916148Notes

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].CS(C)(=O)=O.O1[CH2:49][CH2:48]OCC1>>[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:19]3[CH2:20][CH2:21][N:22]([C:49]4[CH:48]=[CH:8][CH:7]=[CH:6][N:5]=4)[CH2:23][CH2:18]3)[N:13]=2)[CH2:6]1)(=[O:3])=[O:4]

Participants

Reactant 3

HCID 6213Dimethyl Sulfone

HCID 312751,4-Dioxane

HCID 58177355HCID 58177355, compound

Product 1

HCID 69810538HCID 69810538, compound

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 1,1-pyridin-2-yl-piperazine was used to displace the methylsulfone similar to examples above and the de-protection step was similar to step 5, Example 76, to give ((S)-1-methanesulfonyl-piperidin-3-yl)-[2-(4-pyridin-2-yl-piperazin-1-yl)-5-(5H-pyrrolo[2,3-b]pyrazin-2-yl)-pyrimidin-4-yl]-amine. MS: (ES+): 535

Sources & evidence

ORD record: ord-ea6beb326e6a4d158f7ecfcc3fd76386
Source dataset: uspto-grants-2013_12
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08618103B2

Reaction notes

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