HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 5-Amino-2-methylthio-4-(3-aminophenyl)-quinazoline-6-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 5-Amino-2-methylthio-4-(3-aminophenyl)-quinazoline-6-carboxylate | HCID 21109079 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 5-Amino-2-methylthio-4-(3-aminophenyl)-quinazoline-6-carboxylic acid | HCID 21109080 | — |
Reaction Steps
A solution of 5-amino-2-methylthio-4-(3-aminophenyl)-quinazoline-6-carboxylate (example 27f, 658 mg) in 1,4-dioxane was treated with an aqueous solution of KOH (2 M, 4.2 ml) at 70° C. for 18 h. After the reaction mixture was cooled to room temperature, it was acidified to pH 1 with 4 N HCl. The mixture was extracted with CH2Cl2 (3×). The combined organic layers were dried (MgSO4) and concentrated under reduced pressure to give the crude title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07229990B2 |
| Source dataset | uspto-grants-2007_06 |
| ORD ID | ord-cd17b78f5f774fe1bd7952601a89a6cb |
| Source note | uspto-grants-2007_06 |