HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → {1-[(5-Chloro-2,4-dimethoxy-phenylcarbamoyl)-methyl]-2-oxo-1,4-dihydro-2H-quinazolin-3-yl}-acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | {1-[(5-chloro-2,4-dimethoxy-phenylcarbamoyl)-methyl]-2-oxo-1,4-dihydro-2H-quinazolin-3-yl}-acetic acid methyl ester | HCID 68591529 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | {1-[(5-Chloro-2,4-dimethoxy-phenylcarbamoyl)-methyl]-2-oxo-1,4-dihydro-2H-quinazolin-3-yl}-acetic acid | HCID 59317691 | — |
Reaction Steps
An off-white suspension of {1-[(5-chloro-2,4-dimethoxy-phenylcarbamoyl)-methyl]-2-oxo-1,4-dihydro-2H-quinazolin-3-yl}-acetic acid methyl ester (Intermediate I) (400 mg, 0.893 mmol) in MeOH (10 ml) is treated with 5 M KOH (5 ml). The resulting white suspension is left to stir at RT overnight to give clear solution. The aqueous reaction mixture is acidified with dilute HCl (1 M) to pH 4 to give a thick white precipitate which is filtered, washed with water and vacuum dried to afford the title compound as pale yellow solid; [M+H]+ 434.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08633211B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-237ddda454684b4e921beb4893093fab |
| Source note | uspto-grants-2014_01 |