HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → HCID 18473741, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 18473749 | HCID 18473749 | — |
| Solvent | Thionyl Chloride | HCID 24386 | — |
| Product | HCID 18473741 | HCID 18473741 | — |
Reaction Steps
N-{2-[2-(4-Cyanophenyl)-ethyl]-1-methyl-benzimidazol-5-yl}-(4-carboxy-benzenesulphonamide) (2.0 g, 4.3 mmol) is refluxed in 10 mL thionyl chloride for 1.5 h. The mixture is diluted with 50 mL ethyl acetate, the crystalline hydrochloride of the acid chloride is filtered off and washed with ethyl acetate/diethylether. The solid is suspended in 40 mL ethanol and slowly brought to reflux temperature. Half the ethanol is distilled off, the remainder is cooled and combined with ice water and made alkaline with aqueous potassium carbonate solution with stirring. It is diluted with water, the solid is filtered off and washed with water.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06413990B1 |
| Source dataset | uspto-grants-2002_07 |
| ORD ID | ord-d4fe802941ac4bb3ad171437715dc1e7 |
| Source note | uspto-grants-2002_07 |