6-((1R,3r,5S)-3-((5-cyclopropyl-3-(2-(trifluoromethoxy)phenyl)isoxazol-4-yl)methoxy)-8-azabicyclo[3.2.1]oct-8-yl)nicotinic acid

Base Information

Chemical Name:6-((1R,3r,5S)-3-((5-cyclopropyl-3-(2-(trifluoromethoxy)phenyl)isoxazol-4-yl)methoxy)-8-azabicyclo[3.2.1]oct-8-yl)nicotinic acid
CAS No.:1383816-96-3
Molecular Formula:C₂₇H₂₆F₃N₃O₅
Molecular Weight:529.516
Hs Code.:

Synonyms:6-((1R,3r,5S)-3-((5-cyclopropyl-3-(2-(trifluoromethoxy)phenyl)isoxazol-4-yl)methoxy)-8-azabicyclo[3.2.1]oct-8-yl)nicotinic acid

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Chemical Property of 6-((1R,3r,5S)-3-((5-cyclopropyl-3-(2-(trifluoromethoxy)phenyl)isoxazol-4-yl)methoxy)-8-azabicyclo[3.2.1]oct-8-yl)nicotinic acid

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Technology Process of 6-((1R,3r,5S)-3-((5-cyclopropyl-3-(2-(trifluoromethoxy)phenyl)isoxazol-4-yl)methoxy)-8-azabicyclo[3.2.1]oct-8-yl)nicotinic acid

There total 5 articles about 6-((1R,3r,5S)-3-((5-cyclopropyl-3-(2-(trifluoromethoxy)phenyl)isoxazol-4-yl)methoxy)-8-azabicyclo[3.2.1]oct-8-yl)nicotinic acid which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 1383816-95-2
methyl 6-((1R,3r,5S)-3-((5-cyclopropyl-3-(2-(trifluoromethoxy)phenyl)isoxazol-4-yl)methoxy)-8-azabicyclo[3.2.1]oct-8-yl)nicotinate

: 1383816-96-3
6-((1R,3r,5S)-3-((5-cyclopropyl-3-(2-(trifluoromethoxy)phenyl)isoxazol-4-yl)methoxy)-8-azabicyclo[3.2.1]oct-8-yl)nicotinic acid

Guidance literature:: With water; sodium hydroxide; In tetrahydrofuran; methanol; at 50 ℃; for 4h;

Reference yield:

: 1103500-32-8
methyl 5-cyclopropyl-3-(2-(trifluoromethoxy)phenyl)isoxazole-4-carboxylate

: 1383816-96-3
6-((1R,3r,5S)-3-((5-cyclopropyl-3-(2-(trifluoromethoxy)phenyl)isoxazol-4-yl)methoxy)-8-azabicyclo[3.2.1]oct-8-yl)nicotinic acid

Guidance literature:: Multi-step reaction with 6 steps

1: diisobutylaluminium hydride / tetrahydrofuran / -10 - 25 °C

2: 1,2,3-Benzotriazole; thionyl chloride / dichloromethane / 6.5 h / -5 - 25 °C

3: 18-crown-6 ether; potassium tert-butylate / tetrahydrofuran / 0 - 25 °C

4: hydrogenchloride / dichloromethane; 1,4-dioxane / 25 °C

5: caesium carbonate / dimethyl sulfoxide / 4 h / 25 - 80 °C

6: water; sodium hydroxide / tetrahydrofuran; methanol / 4 h / 50 °C

With hydrogenchloride; 1,2,3-Benzotriazole; thionyl chloride; 18-crown-6 ether; potassium tert-butylate; water; diisobutylaluminium hydride; caesium carbonate; sodium hydroxide; In tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane; dimethyl sulfoxide;

Reference yield:

: (5-cyclopropyl-3-(2-(trifluoromethoxy)phenyl)isoxazol-4-yl)-methanol

: 1383816-96-3
6-((1R,3r,5S)-3-((5-cyclopropyl-3-(2-(trifluoromethoxy)phenyl)isoxazol-4-yl)methoxy)-8-azabicyclo[3.2.1]oct-8-yl)nicotinic acid

Guidance literature:: Multi-step reaction with 5 steps

1: 1,2,3-Benzotriazole; thionyl chloride / dichloromethane / 6.5 h / -5 - 25 °C

2: 18-crown-6 ether; potassium tert-butylate / tetrahydrofuran / 0 - 25 °C

3: hydrogenchloride / dichloromethane; 1,4-dioxane / 25 °C

4: caesium carbonate / dimethyl sulfoxide / 4 h / 25 - 80 °C

5: water; sodium hydroxide / tetrahydrofuran; methanol / 4 h / 50 °C

With hydrogenchloride; 1,2,3-Benzotriazole; thionyl chloride; 18-crown-6 ether; potassium tert-butylate; water; caesium carbonate; sodium hydroxide; In tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane; dimethyl sulfoxide;