2-Acetamido-1,3-thiazole-5-sulfonyl chloride → 3-(2-Acetamido-5-thiazolesulfonamido)-2-(2,4-dichlorophenyl)-1-(1H-1,2,4-triazol-1-yl)propan-2-ol
Reaction equation
[NH2:1][CH2:2][C:3]([C:11]1[CH:16]=[CH:15][C:14]([Cl:17])=[CH:13][C:12]=1[Cl:18])([OH:10])[CH2:4][N:5]1[CH:9]=[N:8][CH:7]=[N:6]1.[C:19]([NH:22][C:23]1[S:24][C:25]([S:28](Cl)(=[O:30])=[O:29])=[CH:26][N:27]=1)(=[O:21])[CH3:20]>>[C:19]([NH:22][C:23]1[S:24][C:25]([S:28]([NH:1][CH2:2][C:3]([C:11]2[CH:16]=[CH:15][C:14]([Cl:17])=[CH:13][C:12]=2[Cl:18])([OH:10])[CH2:4][N:5]2[CH:9]=[N:8][CH:7]=[N:6]2)(=[O:29])=[O:30])=[CH:26][N:27]=1)(=[O:21])[CH3:20]Participants
3
Procedure
Following the procedure described in the preceeding examples but using 3-amino-2-(2,4-dichlorophenyl)-1-(1H-1,2,4-triazol-1-yl)propan-2-ol and 2-acetamido-5-thiazolesulfonylchloride, the title compound was obtained in a similar yield:
Sources & evidence
- ORD record
- ord-e9e61fde79254bfdb9de62f2c2096893
- Source dataset
- uspto-grants-1994_11
- Patent number
- US05360813
Reaction notes
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