HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252537Generated: October 30, 2026
Cesium fluoride → HCID 59425912, compound
https://huagongshe.com/reaction/252537
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium fluoride | HCID 25953 | — |
| Reactant | Thiophene-3-boronic acid | HCID 581760 | — |
| Reactant | 5-Bromo-1-ethyl-1H-indole-3-carbonitrile | HCID 57355049 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 59425912 | HCID 59425912 | 25% |
Reaction Steps
A tube is charged with a mixture of 5-bromo-1-ethyl-1H-indole-3-carbonitrile (100 mg, 0.40 mmol), thiophene-3-boronic acid (72 mg, 0.56 mmol), PdCl2(PPh3)2 (11 mg, 0.016 mmol) and CsF (152 mg, 1 mmol) and then alternately evacuated and filled with nitrogen (3×) and diluted with dimethoxyethane (3 mL) and then heated to 90° C. for 19 h. After cooling, the crude reaction mixture is diluted with saturated NaHCO3 and extracted with EtOAc (2×). The combined organic phases are washed with saturated NaCl and dried and concentrated. Flash chromatography over silica gel (CH2Cl2/hexanes, 40/60) gives 25 mg (25%) of 1-ethyl-5-thiophen-3-yl-1H-indole-3-carbonitrile as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07868037B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-97c7db86f2614b32b754b25608535894 |
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| Source note | uspto-grants-2011_01 |
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