1-Methyl-1H-pyrazole-5-sulfonyl chloride → HCID 59578083, compound

HRID 2194164Notes

Reaction equation

HRID 2194164 reaction equation
C(O)(=O)C.[F:5][C:6]([F:26])([F:25])[O:7][C:8]1[CH:13]=[CH:12][C:11]([N:14]2[CH2:18][CH2:17][C:16]3([CH2:23][CH2:22][NH:21][CH2:20][CH2:19]3)[C:15]2=[O:24])=[CH:10][CH:9]=1.[CH3:27][N:28]1[C:32]([S:33](Cl)(=[O:35])=[O:34])=[CH:31][CH:30]=[N:29]1>>[CH3:27][N:28]1[C:32]([S:33]([N:21]2[CH2:20][CH2:19][C:16]3([C:15](=[O:24])[N:14]([C:11]4[CH:12]=[CH:13][C:8]([O:7][C:6]([F:5])([F:25])[F:26])=[CH:9][CH:10]=4)[CH2:18][CH2:17]3)[CH2:23][CH2:22]2)(=[O:35])=[O:34])=[CH:31][CH:30]=[N:29]1

Participants

3

Reactant 2

HCID 224726211-Methyl-1H-pyrazole-5-sulfonyl chlorideHCID 667873332-(4-Trifluoromethoxy-phenyl)-2,8-diaza-spiro[4.5]decan-1-one acetic acid salt

Product 1

HCID 59578083HCID 59578083, compound

Procedure

The title compound was prepared in analogy to example 180 step D from 2-(4-trifluoromethoxy-phenyl)-2,8-diaza-spiro[4.5]decan-1-one acetic acid salt (described in example 180 step C) and 2-methyl-2H-pyrazole-3-sulfonyl chloride. Off-white solid. MS (ESI): 459.3 (MH+)

Sources & evidence

ORD record
ord-9df22d97eef74523a958f38ec531e416
Source dataset
uspto-grants-2012_12
Patent number
US08329904B2

Reaction notes

Loading…