HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-Acetyl-N-[(4-methylquinazolin-2-yl)aminocarbonyl]benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | N-[(4-Methylquinazolin-2-yl)aminocarbonyl]-2-carboxybenzenesulfonamide | HCID 20536263 | — |
| Reactant | HCID 178418348 | HCID 178418348 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Acetyl-N-[(4-methylquinazolin-2-yl)aminocarbonyl]benzenesulfonamide | HCID 20536259 | — |
Reaction Steps
A mixture containing 0.86 g of N-[(4-methylquinazolin-2-yl)aminocarbonyl]-2-carboxybenzenesulfonamide in 50 ml of anhydrous tetrahydrofuran is treated with 40 ml of a 1.4 M solution of methyllithium in ether at 25° under a nitrogen atmosphere. The mixture is stirred for 4 hours at ambient temperature and then poured into 500 ml of water containing 10 ml of concentrated hydrochloric acid. The product can be isolated by extraction into methylene chloride followed by evaporation and if necessary, can be purified by preparative thin layer chromatography and/or recrystallization.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04333760 |
| Source dataset | uspto-grants-1982_06 |
| ORD ID | ord-6e969edd3f8444ca9ced5c613cc35a6d |
| Source note | uspto-grants-1982_06 |