HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1810096Generated: October 31, 2026
Potassium Carbonate → HCID 68510552, compound
https://huagongshe.com/reaction/1810096
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Tert-butyl 2-(3-cyano-4-fluorophenyl)acetate | HCID 45925946 | — |
| Reactant | HCID 63717114 | HCID 63717114 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 68510552 | HCID 68510552 | 48.82% |
Reaction Steps
To a mixture of tert-butyl 2-(3-cyano-4-fluorophenyl)acetate (0.150 g, 0.6376 mmol) and N-(4-chlorophenethyl)-1H-indole-5carboxamide (0.2095 g, 0.7014 mmol) in DMSO (3 mL) was added K2CO3 (0.1322 g, 0.9564 mmol), and the reaction mixture was heated at 120° C. for 30 minutes, then at 130° C. for 1 hour. The reaction was diluted with ethyl acetate and the organic layer was washed with water and brine, dried over magnesium sulfate and concentrated. The residue was purified by silica gel chromatography eluting with a gradient of 5% to 100% ethyl acetate/hexanes to provide tert-butyl 2-(4-(5-((4-chlorophenethyl)carbamoyl)-1H-indol-1-yl)-3cyanophenyl)acetate (0.160 g, 48.82% yield) as a waxy solid. MS (APCI)=514.0 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08362056B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-339b430e8337425e8f1492408092213f |
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| Source note | uspto-grants-2013_01 |
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