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

Base Information

Chemical Name: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
CAS No.:1383816-95-2
Molecular Formula:C₂₈H₂₈F₃N₃O₅
Molecular Weight:543.543
Hs Code.:

Synonyms: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

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Chemical Property of 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

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Technology Process of 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

There total 5 articles about 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 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:

: 1383822-31-8
(1R,3S,5S)-3-({5-cyclopropyl-3-[2-(trifluoromethoxy)phenyl]-1,2-oxazol-4-yl}methoxy)-8-azabicyclo[3.2.1]octane

: 1427-06-1
methyl 6-fluoropyridine-3-carboxylate

: 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

Guidance literature:: With caesium carbonate; In dimethyl sulfoxide; at 25 - 80 ℃; for 4h;

Reference yield:

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

: 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

Guidance literature:: Multi-step reaction with 5 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

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

Reference yield:

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

: 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

Guidance literature:: Multi-step reaction with 4 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

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