HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1192492Generated: November 1, 2026
Ethyl Acetate → 1-[5-Chloro-8-(2-fluorophenyl)quinolin-7-yl]ethanamine
https://huagongshe.com/reaction/1192492
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Trimethylphosphine | HCID 68983 | — |
| Reactant | 7-(1-Azidoethyl)-5-chloro-8-(2-fluorophenyl)quinoline | HCID 86656174 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-[5-Chloro-8-(2-fluorophenyl)quinolin-7-yl]ethanamine | HCID 67248648 | — |
Reaction Steps
To a stirred solution of 7-(1-azidoethyl)-5-chloro-8-(2-fluorophenyl)quinoline (0.037 g, 0.11 mmol) in tetrahydrofuran (0.3 mL) and water (0.0813 mL) was added 1.00 M trimethylphosphine in tetrahydrofuran (0.135 mL, 0.135 mmol) at room temperature and the mixture was stirred at room temperature for 1 hour. To the mixture was added ethyl acetate and the mixture was extracted with 1 N HCl twice. The combined extracts were neutralized with solid sodium bicarbonate, and extracted with dichloromethane. The combined organic layers were washed with brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue showed two peaks by LCMS with the same desired mass and was used directly in the next step (28 mg, 82%). LCMS calculated for C17H15ClFN2(M+H)+: m/z=301.1; found: 301.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08680108B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-4f026b5251ab443abf5a5c9c70983bcd |
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| Source note | uspto-grants-2014_03 |
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