2-Propanesulfonyl chloride → HCID 68565821, compound

HRID 1786493Notes

Reaction equation

HRID 1786493 reaction equation
Cl.[F:2][CH:3]([F:32])[CH2:4][N:5]1[C:13]2[C:8](=[CH:9][C:10]([O:14][CH:15]3[CH2:20][CH2:19][N:18]([CH:21]([CH3:23])[CH3:22])[CH2:17][CH2:16]3)=[CH:11][CH:12]=2)[CH:7]=[C:6]1[C:24]([N:26]1[CH2:31][CH2:30][NH:29][CH2:28][CH2:27]1)=[O:25].[CH3:33][CH:34]([S:36](Cl)(=[O:38])=[O:37])[CH3:35]>>[F:32][CH:3]([F:2])[CH2:4][N:5]1[C:13]2[C:8](=[CH:9][C:10]([O:14][CH:15]3[CH2:20][CH2:19][N:18]([CH:21]([CH3:23])[CH3:22])[CH2:17][CH2:16]3)=[CH:11][CH:12]=2)[CH:7]=[C:6]1[C:24]([N:26]1[CH2:27][CH2:28][N:29]([S:36]([CH:34]([CH3:35])[CH3:33])(=[O:38])=[O:37])[CH2:30][CH2:31]1)=[O:25]

Participants

3

Reactant 2

HCID 824082-Propanesulfonyl chlorideHCID 68563633HCID 68563633, compound

Product 1

HCID 68565821HCID 68565821, compound

Procedure

The title compound was prepared in analogy to example 51, from [1-(2,2-difluoro-ethyl)-5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]-piperazin-1-yl-methanone hydrochloride and 2-propanesulfonyl chloride. Light-yellow solid. MS (m/z): 541.3 (M+H)+.

Sources & evidence

ORD record
ord-cfb1338ead364847928af1d93d45ec38
Source dataset
uspto-grants-2009_03
Patent number
US07507736B2

Reaction notes

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