HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 656059Generated: October 27, 2026
Triethylamine → 5-Bromo-3-[(1,1-dioxidotetrahydro-3-thienyl)methyl]-1H-indole-7-carboxamide
https://huagongshe.com/reaction/656059
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| Reactant | Ammonia methanol | HCID 21705897 | — |
| Reactant | 5-bromo-3-[(1,1-dioxidotetrahydro-3-thienyl)methyl]-1H-indole-7-carboxylic acid | HCID 59332783 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Bromo-3-[(1,1-dioxidotetrahydro-3-thienyl)methyl]-1H-indole-7-carboxamide | HCID 59332621 | 33.6% |
Reaction Steps
TBTU (5.68 g, 17.68 mmol) and triethylamine (1.79 g, 17.68 mmol) were added to a solution of 5-bromo-3-[(1,1-dioxidotetrahydro-3-thienyl)methyl]-1H-indole-7-carboxylic acid (3.28 g, 8.84 mmol) in dichloromethane (100 mL). After the mixture was stirred for 0.5 h at 20° C., NH3/MeOH was added into the solution, and stirring continued for 2 h. The mixture was washed with water and extracted with EtOAc. The organic phase was dried (Na2SO4) and concentrated under reduced pressure. The crude product was purified by column chromatography on silica gel (petroleum:ethyl acetate=10:1 to 5:1 to 2:1), giving 1.1 g (33.6%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08071584B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-2645c6c8a78d47cfb62d345a4029a5ac |
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| Source note | uspto-grants-2011_12 |
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