HuagongsheHuagongshe Chemistry Print Report · For research reference only
Guanidine Hydrochloride → 2-Amino-7-(2-methoxy-phenyl)-7,8-dihydro-6H-quinazolin-5-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Guanidine Hydrochloride | HCID 5742 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-amino-7-(4-chlorophenyl)-7,8-dihydroquinazolin-5(6H)-one | HCID 2772371 | — |
| Reactant | 2-Dimethylaminomethylene-5-(2-methoxy-phenyl)-cyclohexane-1,3-dione | HCID 58269377 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Amino-7-(2-methoxy-phenyl)-7,8-dihydro-6H-quinazolin-5-one | HCID 58269396 | — |
Reaction Steps
The title compound was prepared from 2-dimethylaminomethylene-5-(2-methoxy-phenyl)-cyclohexane-1,3-dione (484 mg, 1.77 mmol) from stage 1, guanidine hydrochloride (253 mg, 2.55 mmol) and sodium carbonate (469 mg, 4.42 mmol), following the procedure described for the synthesis of 2-amino-7-(4-chloro-phenyl)-7,8-dihydro-6H-quinazolin-5-one (example 2/a stage 2) except that the mixture was heated at reflux for 2 h. The reaction mixture was cooled to ambient temperature; water (5 ml) was then added. The precipitate formed was filtered and washed with water (5 ml) to afford the title molecule as a brown powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08592430B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-ef722b14caa5476184af65bd66d97523 |
| Source note | uspto-grants-2013_11 |