Ammonia → HCID 22901846, compound
Reaction equation
[NH3:1].[O:2]=[C:3]1[N:7]([CH2:8][C:9]([C:11]([CH3:14])([CH3:13])[CH3:12])=O)[N:6]=C(C(F)(F)F)O1>C(#N)C>[NH2:6][N:7]1[CH:8]=[C:9]([C:11]([CH3:14])([CH3:13])[CH3:12])[NH:1][C:3]1=[O:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
75 ml of aqueous ammonia solution (25%) are added to a solution of 25.6 g of 2,3-dihydro-2-oxo-3-tert-butylcarbonylmethyl-5-trifluoromethyl-1,3,4-oxadiazole in 100 ml of acetonitrile. After the slightly exothermal reaction has subsided, the reaction mixture is stirred for 2 hours at room temperature and then for 14 hours at 80° and then evaporated, the residue is treated with trichloromethane, and the trichloromethane mixture is freed from the undissolved components, dried and evaporated. The residue is triturated with diethyl ether and subjected to filtration with suction. This gives the tide compound in the form of pale yellow crystals which melt at 197-200°.
Workup
- customAfter the slightly exothermal reaction
- waitfor 14 hours at 80°
- customevaporated
- additionthe residue is treated with trichloromethane
- customdried
- customevaporated
- customThe residue is triturated with diethyl ether
- filtrationsubjected to filtration with suction
- customThis gives the tide compound in the form of pale yellow crystals which
- custommelt at 197-200°
Sources & evidence
- ORD record
- ord-db5ab8838ec64cbbbff27bb96b0b7658
- Source dataset
- uspto-grants-1997_10
- Patent number
- US05679623
Reaction notes
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