Réaction #5474

Équation de réaction

1-azabicyclo[3.3.1]nonane-5-methanamine

5-chloro-2-methoxy-4-(methylamino)benzoic acid

1,1'-carbonyldiimidazole

→

colorless crystals

Rendement 73.3%

N-(1-Azabicyclo[3.3.1]non-5-ylmethyl)-5-chloro-2-methoxy-4-(methylamino)benzamide

Rendement 73.3%

Solvants

tetrahydrofuran

methanol

tetrahydrofuran

Conditions de réaction

Traitement

1. 1
   Autredegassed under a stream of nitrogen for 10 minutes
2. 2
   workup.STIRRINGstirring
3. 3
   workup.WAITwas continued at room temperature for 18 hours
4. 4
   workup.DISSOLUTIONto dissolve the solid
5. 5
   Filtrationthe solution was filtered through a short column of alumina (eluted with 20% methanol/tetrahydrofuran)
6. 6
   ConcentrationThe filtrate was concentrated in vacuo
7. 7
   Autretriturated from cold ether
8. 8
   Autrerecrystallized from acetonitrile

Mode opératoire

A solution of 5-chloro-2-methoxy-4-(methylamino)benzoic acid (1.08 g, 5 mmol) in anhydrous tetrahydrofuran (7 mL) under nitrogen was treated with 1,1'-carbonyldiimidazole (0.90 g, 5.5 mmol), stirred one hour, degassed under a stream of nitrogen for 10 minutes, and cooled (0° C.). A solution of 1-azabicyclo[3.3.1]nonane-5-methanamine (0.82 g, 5.3 mmol) in tetrahydrofuran (3 mL) was added dropwise, and stirring was continued at room temperature for 18 hours. The suspension was diluted with enough methanol to dissolve the solid, then the solution was filtered through a short column of alumina (eluted with 20% methanol/tetrahydrofuran). The filtrate was concentrated in vacuo, triturated from cold ether, and recrystallized from acetonitrile to afford 1.29 g (73%) of colorless crystals; mp 188°-190° C. (second phase), first phase melting point 175° C.

Source