Methyl formate → N-(5-(trifluoromethyl)-1H-indazol-3-yl)formamide
Reaction equation
[NH2:1][C:2]1[C:10]2[C:5](=[CH:6][CH:7]=[C:8]([C:11]([F:14])([F:13])[F:12])[CH:9]=2)[NH:4][N:3]=1.[CH:15](OC)=[O:16]>>[CH:15]([NH:1][C:2]1[C:10]2[C:5](=[CH:6][CH:7]=[C:8]([C:11]([F:12])([F:14])[F:13])[CH:9]=2)[NH:4][N:3]=1)=[O:16]Participants
3
Procedure
A mixture of 5.0 g. of 3-amino-5-trifluoromethylindazole, prepared as in Example 1, and 25 ml. of methyl formate is refluxed for eight hours, then concentrated in vacuo to leave crude 3-formylamino-5-trifluoromethylindazole.
Workup
- additionA mixture of 5.0 g
- concentrationconcentrated in vacuo
Sources & evidence
- ORD record
- ord-b16303dcfe42434785e99c0fe796184f
- Source dataset
- uspto-grants-1976_08
- Patent number
- USRE028939
Reaction notes
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