N-(2,4-Dimethylthiophen-3-yl)-N-n-propylcarbamoyl chloride → N-(2,4-Dimethylthiophen-3-yl)-N-n-propyl-4,5-dihydro-4-(2-fluoro-phenyl)-1H-tetrazol-5-one-1-carboxamide
Reaction equation
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[N:8]1[C:12](=[O:13])[N:11]=[N:10][NH:9]1.[CH3:14][C:15]1[S:16][CH:17]=[C:18]([CH3:27])[C:19]=1[N:20]([CH2:24][CH2:25][CH3:26])[C:21](Cl)=[O:22]>CN(C)C1C=CN=CC=1>[CH3:14][C:15]1[S:16][CH:17]=[C:18]([CH3:27])[C:19]=1[N:20]([CH2:24][CH2:25][CH3:26])[C:21]([N:11]1[C:12](=[O:13])[N:8]([C:3]2[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=2[F:1])[N:9]=[N:10]1)=[O:22]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
1.17 g (6.5 mmol) of 1,2-dihydro-1-(2-fluorophenyl)-5H-tetrazol-5-one, 1.5 g (6.5 mmol) of N-(2,4-dimethyl-thiophen-3-yl)-N-n-propylcarbamoyl chloride and 1.19 g (9.7 mmol) of 4-dimethylaminopyridine were reacted by the method of the process described in Example 1. Yield 1.9 g.
Sources & evidence
- ORD record
- ord-38041aabf37b4880a244b1a4c13767e3
- Source dataset
- uspto-grants-2001_08
- Patent number
- US06277790B1
Reaction notes
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