Triethylamine → 5-amino-1H-pyrazole-1-carboxamide
Reaction equation
[C:1]([CH:3]=[CH:4][NH:5][NH:6][C:7]([NH2:9])=[O:8])#[N:2].C(N(CC)CC)C>C(O)C>[NH2:2][C:1]1[N:6]([C:7]([NH2:9])=[O:8])[N:5]=[CH:4][CH:3]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 5.0 g of the product of Example 13 in 50 ml of ethyl alcohol containing 3.0 ml of triethylamine is heated at reflux for 4 hours then concentrated in vacuo to a residue which is stirred with cold water. The resulting solid is filtered, washed with additional cold water and dried to give 4.0 g of the desired product as a yellow crystalline solid. M+H=127.
Workup
- temperatureat reflux for 4 hours
- concentrationthen concentrated in vacuo to a residue which
- filtrationThe resulting solid is filtered
- washwashed with additional cold water
- customdried
Sources & evidence
- ORD record
- ord-b430d70547d54932b594d394fd92d52e
- Source dataset
- uspto-grants-1994_10
- Patent number
- US05358947
Reaction notes
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