HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 2-[1-(4-chlorobenzyl)-1H-indol-3-yl]-2-oxo-N-(5-oxo-2,5-dihydro-3-thienyl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(1-(4-chlorobenzyl)-1H-indol-3-yl)-2-oxo-acetyl chloride | HCID 10980477 | — |
| Reactant | 5,7-Dimethoxy-1-(4-chlorobenzyl)indole | HCID 22256884 | — |
| Reactant | 4-amino-5H-thiophen-2-one | HCID 23514080 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 2-[1-(4-chlorobenzyl)-1H-indol-3-yl]-2-oxo-N-(5-oxo-2,5-dihydro-3-thienyl)acetamide | HCID 23514042 | — |
Reaction Steps
A suspension of 4-amino-5H-thiophen-2-one of Preparation 5 (103 mg), powdered potassium carbonate (138 mg) and 2-(1-(4-chlorobenzyl)-1H-indol-3-yl)-2-oxo-acetyl chloride of Example 1 (334 mg) in 1,2-dimethoxyethane (5 ml) is stirred at room temperature for 2 h. After this time the reaction mixture is poured in water (50 ml) and the obtained precipitate is collected by filtration and thoroughly washed with water. The still wet solid is suspended in methanol and stirred for 30′. Filtration followed by drying at 40° C. under vacuum gives 2-[1-(4-chlorobenzyl)-1H-indol-3-yl]-2-oxo-N-(5-oxo-2,5-dihydro-3-thienyl)acetamide (280 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06753342B2 |
| Source dataset | uspto-grants-2004_06 |
| ORD ID | ord-2b4124f0d6124809b3de884b5fbdbcec |
| Source note | uspto-grants-2004_06 |