HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 7-(4-Bromo-2-chlorophenylamino)-8-fluoro-4-methylquinazoline-6-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | 7-(4-Bromo-2-chlorophenylamino)-8-fluoro-4-methylquinazoline-6-carboxylic acid methyl ester | HCID 68637503 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Oxolane--water (1/1) | HCID 21881883 | — |
| Product | 7-(4-Bromo-2-chlorophenylamino)-8-fluoro-4-methylquinazoline-6-carboxylic acid | HCID 68637208 | 73% |
Reaction Steps
To a solution of 7-(4-bromo-2-chlorophenylamino)-8-fluoro-4-methylquinazoline-6-carboxylic acid methyl ester (137 mg, 0.323 mmol) in THF-water (3 mL/l mL) was added 1 M aqueous LiOH (0.67 mL, 0.67 mmol) at room temperature. The resulting mixture was stirred for 2 hours at room temperature. The reaction mixture was acidified to pH 6 with 1 N aqueous HCl, diluted with water, and extracted with EtOAc. The organic layer was washed with water, dried over MgSO4, filtered, and concentrated in vacuo to give the desired product (96 mg, 73%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07772234B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-e8a98afc5f0349adb5a106f2f84aca04 |
| Source note | uspto-grants-2010_08 |