Benzenesulfonamide, 3-amino-N-phenyl- → HCID 11707055, compound

HRID 2224473Notes

Reaction equation

HRID 2224473 reaction equation
[F:1][C:2]([F:26])([F:25])[C:3]1[N:8]2[N:9]=[CH:10][C:11]([C:12](O)=[O:13])=[C:7]2[N:6]=[C:5]([C:15]2[CH:20]=[CH:19][C:18]([C:21]([F:24])([F:23])[F:22])=[CH:17][CH:16]=2)[CH:4]=1.[NH2:27][C:28]1[CH:29]=[C:30]([S:34]([NH:37][C:38]2[CH:43]=[CH:42][CH:41]=[CH:40][CH:39]=2)(=[O:36])=[O:35])[CH:31]=[CH:32][CH:33]=1>>[C:38]1([NH:37][S:34]([C:30]2[CH:29]=[C:28]([NH:27][C:12]([C:11]3[CH:10]=[N:9][N:8]4[C:3]([C:2]([F:25])([F:1])[F:26])=[CH:4][C:5]([C:15]5[CH:16]=[CH:17][C:18]([C:21]([F:22])([F:23])[F:24])=[CH:19][CH:20]=5)=[N:6][C:7]=34)=[O:13])[CH:33]=[CH:32][CH:31]=2)(=[O:35])=[O:36])[CH:39]=[CH:40][CH:41]=[CH:42][CH:43]=1

Participants

3

Procedure

The title compound was prepared from 7-trifluoromethyl-5-(4-trifluoromethyl-phenyl)-pyrazolo[1,5-a]pyrimidine-3-carboxylic acid (example C.2) and 3-amino-N-phenyl-benzenesulfonamide [commercially available] according to general procedure II. Yellow solid. MS (ISP) 604.0 [(M−H)−]; mp 258° C.

Sources & evidence

ORD record
ord-8155365db8ac48ee8ec6b3302af49c1e
Source dataset
uspto-grants-2008_05
Patent number
US07378417B2

Reaction notes

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