HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1031487Generated: October 31, 2026
2-Bromo-3-methoxypyridine → 2-(3-methoxy-2-pyridinyl)-5-phenylmethyl-(1S,4S)-2,5-diazabicyclo[2.2.1]-heptane
https://huagongshe.com/reaction/1031487
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromo-3-methoxypyridine | HCID 90364 | — |
| Reactant | (1S,4S)-2-Benzyl-2,5-Diazabicyclo[2.2.1]heptane | HCID 14612543 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(3-methoxy-2-pyridinyl)-5-phenylmethyl-(1S,4S)-2,5-diazabicyclo[2.2.1]-heptane | HCID 18640952 | 51% |
Reaction Steps
A mixture of 2-bromo-3-methoxy pyridine (9.9 g) and (1S,4S)-N-benzyl-2,5-diazabicyclo[2.2.1]heptane (10.9 g) was heated at 100° C. in a Parr bomb for 67 h. The reaction mixture was cooled to 23° C., dissolved in CH2Cl2, extracted with 5% NaHCO3, and finally wit:h H2O. The organic layer was dried over K2CO3, filtered, and concentrated under reduced pressure. The crude oil was purified by silica gel chromatography (CH2Cl2 :MeOH; 96:4) to give the desired product (7.93 g, 51%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04954502 |
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| Source dataset | uspto-grants-1990_09 |
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| ORD ID | ord-c33d51057ad54739892d9bc674b95593 |
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| Source note | uspto-grants-1990_09 |
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