HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 72437Generated: October 25, 2026
Triethylamine → Methyl 5-chloro-2-(3-phenoxyazetidin-1-yl)nicotinate
https://huagongshe.com/reaction/72437
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methyl 2,5-Dichloronicotinate | HCID 2764318 | — |
| Reactant | 3-Phenoxyazetidine | HCID 12812501 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 5-chloro-2-(3-phenoxyazetidin-1-yl)nicotinate | HCID 67958085 | 74.7% |
Reaction Steps
To a solution of methyl 2,5-dichloronicotinate (217 mg, 1.05 mmol) in tetrahydrofuran (5 ml), 3-phenoxyazetidine (D48) (149 mg, 1.05 mmol) and triethylamine (117 mg, 1.16 mmol) were added and the mixture was heated at reflux for 18 hours. The resulting mixture was cooled to room temperature, the precipitates were filtered off and the filtrate was concentrated under vacuo. The residue was dissolved in ethyl acetate (5 ml), washed with water (5 ml) and brine (5 ml), dried over Na2SO4, filtered and concentrated. The crude residue was purified by flash chromatography on silica gel eluting with a mixture petroleum ether/ethyl acetate from 30:1 to 20:1. Collected fractions after solvent evaporation afforded the title compound (D75) (250 mg) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08828987B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-1f25136830aa49c1a30b8108e105b5b3 |
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| Source note | uspto-grants-2014_09 |
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