HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfanilic acid → 4-(7-Trifluoromethyl-4-quinazolinylamino)benzenesulphonic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfanilic acid | HCID 8479 | — |
| Reactant | 4-Chloro-7-(trifluoromethyl)quinazoline | HCID 12806742 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(7-Trifluoromethyl-4-quinazolinylamino)benzenesulphonic acid | HCID 21273953 | — |
Reaction Steps
0.8 grams of sulphanilic acid and an equimolar quantity of 4-chloro-7-trifluoromethylquinazoline were heated in 20 ml of 50% aqueous ethanol at 100° C. for 2 hours. The suspension was cooled and the solid was filtered off, washed with water and dried to give 1.03 g of the title compound. The sulphonyl chloride hydrochloride derivative for use in part (b) below was prepared in similar manner to Examples 1 and 2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04808715 |
| Source dataset | uspto-grants-1989_02 |
| ORD ID | ord-6497545b57964abaae7557ce2fc2a7f1 |
| Source note | uspto-grants-1989_02 |