HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formamidine acetate → HCID 135682057, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formamidine acetate | HCID 160693 | — |
| Reactant | HCID 59015784 | HCID 59015784 | — |
| Solvent | 2-Methoxyethanol | HCID 8019 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 135682057 | HCID 135682057 | — |
Reaction Steps
Heat a solution of 3-amino-2′-trifluoromethyl-biphenyl-4-carboxylic-acid methyl ester (5.0 g, 0.0169 mol) and formamidine acetate (2.8 g, 0.0203 mol) in 2-methoxyethanol at reflux for 8 hours. Cool the mixture and concentrate under reduced pressure to give a dark oil. Dissolve the residue in 10% NaOH and wash the aqueous with ether (3×). Bring the aqueous layer to pH 4 using 12N HCl to produce a milky solution. Extract the solution with EtOAc, wash the EtOAc with brine, dry (Na2SO4) and concentrate under reduced pressure to give 7-(2-Trifluoromethyl-phenyl)-3H-quinazolin-4-one as a beige solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07304059B2 |
| Source dataset | uspto-grants-2007_12 |
| ORD ID | ord-72cc8e53cd814c4a966d82835e61070d |
| Source note | uspto-grants-2007_12 |