HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 57901805, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Ethyl cysteinate hydrochloride | HCID 2723617 | — |
| Reactant | HCID 57901755 | HCID 57901755 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 57901805 | HCID 57901805 | 25.5% |
Reaction Steps
A mixture of N-(2-cyano-1H-indol-7-yl)thiophene-2-sulfonamide (0.30 g), cysteine ethyl ester hydrochloride (0.22 g) and ethanol (10 mL) was heated under reflux overnight. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4) and concentrated. The obtained residue was subjected to silica gel column chromatography and the title compound (0.11 g, yield 25%) was obtained as pale-yellow crystals from a fraction eluted with ethyl acetate-hexane (1:1, volume ratio). The crystals were recrystallized from ethyl acetate-hexane. melting point 156-157° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08957070B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-331e1ea1d3884bf58b687c0fae4c21c5 |
| Source note | uspto-grants-2015_02 |