Back
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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-3-methoxypyridineHCID 90364—
Reactant(1S,4S)-2-Benzyl-2,5-Diazabicyclo[2.2.1]heptaneHCID 14612543—
SolventDichloromethaneHCID 6344—
Product2-(3-methoxy-2-pyridinyl)-5-phenylmethyl-(1S,4S)-2,5-diazabicyclo[2.2.1]-heptaneHCID 1864095251%

Reaction Conditions

Temperature100 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04954502
Source datasetuspto-grants-1990_09
ORD IDord-c33d51057ad54739892d9bc674b95593
Source noteuspto-grants-1990_09