Benzenesulfonamide, 3-amino- → HCID 69293419, compound
Reaction equation
[CH:1]1([C:4]2[N:9]3[N:10]=[CH:11][C:12]([C:13](O)=[O:14])=[C:8]3[N:7]=[C:6]([C:16]3[CH:21]=[CH:20][C:19]([C:22]([F:25])([F:24])[F:23])=[CH:18][CH:17]=3)[CH:5]=2)[CH2:3][CH2:2]1.[NH2:26][C:27]1[CH:28]=[C:29]([S:33]([NH2:36])(=[O:35])=[O:34])[CH:30]=[CH:31][CH:32]=1>>[S:33]([C:29]1[CH:28]=[C:27]([NH:26][C:13]([C:12]2[CH:11]=[N:10][N:9]3[C:4]([CH:1]4[CH2:3][CH2:2]4)=[CH:5][C:6]([C:16]4[CH:21]=[CH:20][C:19]([C:22]([F:25])([F:24])[F:23])=[CH:18][CH:17]=4)=[N:7][C:8]=23)=[O:14])[CH:32]=[CH:31][CH:30]=1)(=[O:34])(=[O:35])[NH2:36]Participants
3
Procedure
The title compound was prepared from 7-cyclopropyl-5-(4-trifluoromethyl-phenyl)-pyrazolo[1,5-a]pyrimidine-3-carboxylic acid (example C.29) and 3-amino-benzenesulfonamide according to general procedure II. Pale-yellow solid. MS (ISP) 502.3 [(M+H)+]; mp 249-250° C.
Sources & evidence
- ORD record
- ord-d0f9f2a4b2fc41e5a3539462e543b0b9
- Source dataset
- uspto-grants-2008_05
- Patent number
- US07378417B2
Reaction notes
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