HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387399Generated: October 27, 2026
Potassium Carbonate → 3-[(1,1-Dioxidotetrahydro-3-thienyl)methyl]-5-(3-thienyl)-1H-indole-7-carboxamide
https://huagongshe.com/reaction/387399
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Thiopheneboronic acid | HCID 2733960 | — |
| Reactant | 5-Bromo-3-[(1,1-dioxidotetrahydro-3-thienyl)methyl]-1H-indole-7-carboxamide | HCID 59332621 | — |
| Catalyst | Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+) | HCID 178418228 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-[(1,1-Dioxidotetrahydro-3-thienyl)methyl]-5-(3-thienyl)-1H-indole-7-carboxamide | HCID 59332710 | 87.3% |
Reaction Steps
5-bromo-3-[(1,1-dioxidotetrahydro-3-thienyl)methyl]-1H-indole-7-carboxamide (40 mg, 0.108 mmol), 2-thienylboronic acid (20.68 mg, 0.162 mmol, 1.5 eq), PdCl2(dppf) (7.88 mg, 10.77 μmol, 0.1 eq), potassium carbonate (44.7 mg, 0.323 mmol, 3 eq) were diluted in a mixture of 1,4-dioxane (3 mL) and water (1 mL), in a 2-5 mL biotage microwave reaction tube. The mixture was degassed by bubbling nitrogen through for 5 minutes and was then heated in a microwave at high absorption for 15 minutes at 120° C. The reaction was filtered through a thiol SPE cartridge (polymer labs) and was concentrated and purified by Gilson HPLC with trifluoroacetic acid buffer. The desired product fractions were combined and concentrated in an EZ2 Genevac evaporator, giving 35.3 mg (82%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08372875B2 |
|---|
| Source dataset | uspto-grants-2013_02 |
|---|
| ORD ID | ord-dabfd389fb764b3a9a20bede49673276 |
|---|
| Source note | uspto-grants-2013_02 |
|---|