Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylacetamide | HCID 31374 | — |
| Reactant | 2-Bromopropanedial | HCID 74945 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 57475964 | HCID 57475964 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 59136021 | HCID 59136021 | 29.4% |
Reaction Steps
7-[(2-Ethoxyethyl) (2-thienylsulfonyl)amino]-1H-indole-2-carbothioamide (3.00 g), bromomalonaldehyde (2.32 g) and N,N-dimethylacetamide (50 mL) were stirred at 95° C. for 3 hr. The reaction mixture was diluted with ethyl acetate and water, and the ethyl acetate layer was washed successively with saturated brine and aqueous sodium bicarbonate, dried over magnesium sulfate and filtrated. The filtrate was concentrated, subjected to silica gel column chromatography and eluted with a mixture of ethyl acetate-hexane (1:1) to give a solid. The solid was dissolved in tetrahydrofuran (50 mL) and methanol (20 mL), sodium borohydride (176 mg) was added and the mixture was stirred at room temperature for 3 days. The reaction mixture was diluted with ethyl acetate and washed with saturated brine. The organic layer was dried over magnesium sulfate and filtrated. The filtrate was concentrated, subjected to silica gel column chromatography and eluted with a mixture of ethyl acetate-hexane (2:1) to give the title compound (1.00 g, yield 29%) as an amorphous form.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08957070B2 |
|---|
| Source dataset | uspto-grants-2015_02 |
|---|
| ORD ID | ord-ca3317fad9be4dfabe2fcec8294d2822 |
|---|
| Source note | uspto-grants-2015_02 |
|---|