1,3,4-Thiadiazol-2-amine → 4-Fluoro-3-nitro-N-[1,3,4]thiadiazol-2-yl-benzamide
Reaction equation
[F:1][C:2]1[CH:10]=[CH:9][C:5]([C:6](Cl)=[O:7])=[CH:4][C:3]=1[N+:11]([O-:13])=[O:12].[S:14]1[CH:18]=[N:17][N:16]=[C:15]1[NH2:19]>>[F:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([NH:19][C:15]2[S:14][CH:18]=[N:17][N:16]=2)=[O:7])=[CH:4][C:3]=1[N+:11]([O-:13])=[O:12]Participants
3
Procedure
The product from Example 172a was reacted with [1,3,4]Thiadiazol-2-ylamine (149 mg, 1.474 mmol) according to the procedure from Example 172b to provide the title compound (272 mg, 67%).
Sources & evidence
- ORD record
- ord-ed2f5c9026ea4eb8a679630cac026aa2
- Source dataset
- uspto-grants-2011_03
- Patent number
- US07910595B2
Reaction notes
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