HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 659953Generated: October 30, 2026
2-Fluoroethyl bromide → HCID 86643499, compound
https://huagongshe.com/reaction/659953
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Fluoroethyl bromide | HCID 12982 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 10871025 | HCID 10871025 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86643499 | HCID 86643499 | 62.8% |
Reaction Steps
Sodium hydride (371 mg, 9.3 mmoles 60% in oil) is added to a solution of 1 g (3.1 mmoles) of 2-(2-Chloro-pyridin-4-yl)-3-(4-fluoro-phenyl)-1H-pyrrolo[3,2-b]pyridine (prepared following the procedure for example 6) in 20 mL of dimethylformamide at room temperature. After 30 min. at room temperature, 2.75 g of 1-bromo-2-fluoro-ethane (21.6 mmoles) is added to the reaction mixture. After 10 hour at room temperature, the reaction mixture is poured into ammonium chloride solution and extracted with ethyl acetate. The organic phase is washed with water and dried over magnesium sulfate. After concentration the solid residue is purified by chromatography on silica gel (ethyl acetate/hexane 1/1) to give 720 mg of 2-(2-Chloro-pyridin-4-yl)-1-(2-fluoro-ethyl)-3-(4-fluoro-phenyl)-1H-pyrrolo[3,2-b]pyridine as white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08084395B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-a2249097ab654673a35db6e03cb522c7 |
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| Source note | uspto-grants-2011_12 |
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