2-[(Trifluoroacetyl)amino]benzamide → 2-(Trifluoromethyl)-3,4-dihydroquinazolin-4-one
Reaction equation
[F:1][C:2]([F:16])([F:15])[C:3]([NH:5][C:6]1[CH:14]=[CH:13][CH:12]=[CH:11][C:7]=1[C:8]([NH2:10])=[O:9])=O>C(O)CO>[F:1][C:2]([F:16])([F:15])[C:3]1[NH:10][C:8](=[O:9])[C:7]2[C:6](=[CH:14][CH:13]=[CH:12][CH:11]=2)[N:5]=1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
(Trifluoroacetamido)benzamide (73.0 g, 0.31 mole) was heated in ethylene glycol (150 ml) in an oil bath with stirring. The amide dissolved at around 130° and product began to precipitate out at 150°. The temperature was held at 150° for a further 1 hour before cooling. The solid was filtered off washing well with cold water to give the product, 55.7 g (84%).
Workup
- customto precipitate out at 150°
- temperaturebefore cooling
- filtrationThe solid was filtered off
- washwashing well with cold water
- customto give the product, 55.7 g (84%)
Sources & evidence
- ORD record
- ord-bfa8134c6fa248d7833d2af504c616c4
- Source dataset
- uspto-grants-1995_05
- Patent number
- US05415981
Reaction notes
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