3-(Morpholine-4-sulfonyl)aniline → 5-(4-Chloro-phenyl)-7-difluoromethyl-pyrazolo[1,5-a]pyrimidine-3-carboxylic acid[3-(morpholine-4-sulfonyl)-phenyl]-amide
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:13]=[C:12]([CH:14]([F:16])[F:15])[N:11]3[N:17]=[CH:18][C:19]([C:20]([OH:22])=O)=[C:10]3[N:9]=2)=[CH:4][CH:3]=1.[N:23]1([S:29]([C:32]2[CH:33]=[C:34]([NH2:38])[CH:35]=[CH:36][CH:37]=2)(=[O:31])=[O:30])[CH2:28][CH2:27][O:26][CH2:25][CH2:24]1>>[N:23]1([S:29]([C:32]2[CH:33]=[C:34]([NH:38][C:20]([C:19]3[CH:18]=[N:17][N:11]4[C:12]([CH:14]([F:16])[F:15])=[CH:13][C:8]([C:5]5[CH:6]=[CH:7][C:2]([Cl:1])=[CH:3][CH:4]=5)=[N:9][C:10]=34)=[O:22])[CH:35]=[CH:36][CH:37]=2)(=[O:31])=[O:30])[CH2:24][CH2:25][O:26][CH2:27][CH2:28]1Participants
3
Procedure
The title compound was prepared from 5-(4-chloro-phenyl)-7-difluoromethyl-pyrazolo[1,5-a]pyrimidine-3-carboxylic acid (example C.3) and 3-(morpholine-4-sulfonyl)-phenylamine [CAS 22184-97-0; commercially available] according to general procedure II. Yellow solid. MS (ISP) 548.3 [(M+H)+]; mp 253° C.
Sources & evidence
- ORD record
- ord-e381df2e9e024acab68206a255f96239
- Source dataset
- uspto-grants-2008_05
- Patent number
- US07378417B2
Reaction notes
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