HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2043462Generated: November 3, 2026
Diisopropylethylamine → HCID 86762130, compound
https://huagongshe.com/reaction/2043462
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | (S)-1-(4-Fluorophenyl)-ethylamine | HCID 2779063 | — |
| Reactant | Methyl 2,6-dichloropyridine-3-carboxylate | HCID 11106516 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86762130 | HCID 86762130 | 37.8% |
Reaction Steps
5.0 g of methyl 2,6-dichloronicotinate was dissolved in ml of dimethylformamide, and 4.39 g of (S)-(−)-1-(4-fluorophenyl)ethylamine, 6.27 g of diisopropylethylamine and 150 mg of 4-dimethylaminopyridine were added thereto, and the mixture was stirred at 60° C. for 24 hours. The reaction solution was cooled, and then diluted with ethyl acetate, and washed in turn with water and brine, and the organic layer was dried over magnesium sulfate. The solvent was distilled off under reduced pressure, and then the obtained residue was purified by silica gel column chromatography to obtain 2.83 g of the objective compound as white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08586591B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-02c21fa0a45b451ca0380f6e0336dcdf |
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| Source note | uspto-grants-2013_11 |
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