HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclohexylthiourea → 7-[2-(Cyclohexylamino)-1,3-thiazol-5-yl]quinazolin-4(3h)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclohexylthiourea | HCID 1471603 | — |
| Reactant | Bromo-(4-oxo-3,4-dihydro-quinazolin-7-yl)acetaldehyde | HCID 135531132 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 7-[2-(Cyclohexylamino)-1,3-thiazol-5-yl]quinazolin-4(3h)-one | HCID 135496165 | — |
Reaction Steps
A solution of bromo-(4-oxo-3,4-dihydro-quinazolin-7-yl)acetaldehyde and N-cyclohexylthiourea in dimethylformamide is heated at 70° C. until completion of the reaction (5-12 hours). The mixture is quenched with 10% dimethylamine in ethanol and the solvent is removed under reduced pressured. The crude is purified by chromatography on silica gel to isolate the desired compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06852720B2 |
| Source dataset | uspto-grants-2005_02 |
| ORD ID | ord-25238562fd52496693cf85f9c426924f |
| Source note | uspto-grants-2005_02 |