HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 445549Generated: October 29, 2026
Pyridine → 2-azetidin-1-yl-5-bromopyridine
https://huagongshe.com/reaction/445549
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Azetidine | HCID 10422 | — |
| Reactant | 5-Bromo-2-chloropyridine | HCID 2734414 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 2-azetidin-1-yl-5-bromopyridine | HCID 18329833 | — |
Reaction Steps
A mixture of 5-bromo-2-chloropyridine (Sigma-Aldrich, Buchs, Switzerland, 196 mg, 1.018 mmol), azetidine (Sigma-Aldrich, Buchs, Switzerland, 0.213 ml, 3.06 mmol) and pyridine (0.124 ml, 1.528 mmol) in DMA (2.5 ml) was heated under microwave irradiation at 150° C. for 10 min and 170° C. for 10 min. The reaction was not completed. Again azetidine (0.106 ml) was added and the RM was heated under microwave irradiation at 170° C. for 1 h. Then the RM was quenched with saturated aqueous NaHCO3 (50 ml) and extracted with EtOAc (2×). The combined organic layers were washed with brine (2×), dried over Na2SO4, filtered and evaporated to dryness to give the title compound as an off-white solid. (HPLC: tR 1.97 min (Method A); M+H=213, 215 (Br-pattern) MS-ES. 1H-NMR (d6-DMSO, 400 MHz) 8.12 (s, 1H), 7.70-7.60 (m, 1H), 6.37-6.29 (m, 1H), 3.96-3.86 (m, 4H), 2.34-2.24 (m, 2H))
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08476294B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-25c6d8240e6342a8aa2c588ef496af37 |
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| Source note | uspto-grants-2013_07 |
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