Methanesulfonyl chloride → HCID 66998057, compound

HRID 559239Notes

Reaction equation

HRID 559239 reaction equation
[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[C:9]1[C:27](=[O:28])[N:26]([CH3:29])[C:12]2[N:13]([CH3:25])[C:14]3[C:19]([C:11]=2[CH:10]=1)=[CH:18][C:17]([C:20]1[NH:21][N:22]=[CH:23][CH:24]=1)=[CH:16][CH:15]=3.[CH3:30][S:31](Cl)(=[O:33])=[O:32]>>[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[C:9]1[C:27](=[O:28])[N:26]([CH3:29])[C:12]2[N:13]([CH3:25])[C:14]3[C:19]([C:11]=2[CH:10]=1)=[CH:18][C:17]([C:20]1[CH:24]=[CH:23][N:22]([S:31]([CH3:30])(=[O:33])=[O:32])[N:21]=1)=[CH:16][CH:15]=3

Participants

3

Reactant 2

HCID 31297Methanesulfonyl chlorideHCID 16226262HCID 16226262, compound

Product 1

HCID 66998057HCID 66998057, compound

Procedure

The process is carried out as indicated in Example 99 above with the compound from Example 39, 3-(2,4-dichlorophenyl)-1,9-dimethyl-6-(2H-pyrazol-3-yl)-1,9-dihydro-pyrido[2,3-b]indol-2-one, and methanesulphonyl chloride.

Sources & evidence

ORD record
ord-8c0081b7ff3e409db2674947c46490bd
Source dataset
uspto-grants-2011_11
Patent number
US08063061B2

Reaction notes

Loading…