Ammonia → 1-Azabicyclo[3.3.1]nonane-5-carboxamide

Temperature

150 °C

A solution of 1-azabicyclo[3.3.1]nonane-5-carboxylic acid methyl ester (1.83 g, 10 mmol) in ammonia (50 mL) and methanol (20 mL) was sealed in a bomb and heated at 120°-130° C. for 36 hours (gas chromatography indicated that the reaction was incomplete). Three drops of 25% sodium methoxide/methanol were added, and the mixture was heated at 130° C. for 21 hours and at 150° C. for 72 hours, at which time the reaction was essentially complete. The solution was concentrated in vacuo and the residue was partitioned between 1.25 N sodium carbonate (50 mL) and methylene chloride (75 mL). The organic layer was separated and the aqueous solution was extracted with methylene chloride (2×40 mL). The combined organic layers were dried (Na2SO4), concentrated in vacuo, and recrystallized from acetonitrile to afford 0.64 g (38%) of pale brown solid: mp 172.5°-175.0° C.

1. temperatureheated at 120°-130° C. for 36 hours (gas chromatography
2. concentrationThe solution was concentrated in vacuo
3. customthe residue was partitioned between 1.25 N sodium carbonate (50 mL) and methylene chloride (75 mL)
4. customThe organic layer was separated
5. extractionthe aqueous solution was extracted with methylene chloride (2×40 mL)
6. dry with materialThe combined organic layers were dried (Na2SO4)
7. concentrationconcentrated in vacuo
8. customrecrystallized from acetonitrile

ORD record

ord-0aaee6cf00dd4c9092fbecc6c457f925

Source dataset

uspto-grants-1993_03

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US05190953