(1R,3s,5S)-tert-butyl 3-((1r,4R)-4-(2-methyl-6-(pyridazin-4-yl)pyridin-3-yloxy)cyclohexyloxy)-8-azabicyclo[3.2.1]octane-8-carboxylate

Base Information

Chemical Name:(1R,3s,5S)-tert-butyl 3-((1r,4R)-4-(2-methyl-6-(pyridazin-4-yl)pyridin-3-yloxy)cyclohexyloxy)-8-azabicyclo[3.2.1]octane-8-carboxylate
CAS No.:1430745-84-8
Molecular Formula:C₂₈H₃₈N₄O₄
Molecular Weight:494.634
Hs Code.:

Synonyms:(1R,3s,5S)-tert-butyl 3-((1r,4R)-4-(2-methyl-6-(pyridazin-4-yl)pyridin-3-yloxy)cyclohexyloxy)-8-azabicyclo[3.2.1]octane-8-carboxylate

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Chemical Property of (1R,3s,5S)-tert-butyl 3-((1r,4R)-4-(2-methyl-6-(pyridazin-4-yl)pyridin-3-yloxy)cyclohexyloxy)-8-azabicyclo[3.2.1]octane-8-carboxylate

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Technology Process of (1R,3s,5S)-tert-butyl 3-((1r,4R)-4-(2-methyl-6-(pyridazin-4-yl)pyridin-3-yloxy)cyclohexyloxy)-8-azabicyclo[3.2.1]octane-8-carboxylate

There total 6 articles about (1R,3s,5S)-tert-butyl 3-((1r,4R)-4-(2-methyl-6-(pyridazin-4-yl)pyridin-3-yloxy)cyclohexyloxy)-8-azabicyclo[3.2.1]octane-8-carboxylate 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: 89.5%

: 1430746-13-6
(1,3s,5S)-tert-btyl 3-((1,4R)4-(6-bromo-2-methylpyridin-3-yloxy)cyclohexyloxy)-8-azabicyclo[3.2.1]octane-8-carboxylate

: 194865-89-9
4-(tributylstannanyl)pyridazine

: 1430745-84-8
(1R,3s,5S)-tert-butyl 3-((1r,4R)-4-(2-methyl-6-(pyridazin-4-yl)pyridin-3-yloxy)cyclohexyloxy)-8-azabicyclo[3.2.1]octane-8-carboxylate

Guidance literature:: With trans-bis(triphenylphosphine)palladium dichloride; In 1,4-dioxane; at 110 ℃; for 16h; Inert atmosphere;

Reference yield:

: 1430746-24-9
(1R,3s,5S)-tert-butyl 3-((1s,4S)-4-hydroxycyclohexyloxy)-8-azabicyclo[3.2.1]octane-8-carboxylate

: 1430745-84-8
(1R,3s,5S)-tert-butyl 3-((1r,4R)-4-(2-methyl-6-(pyridazin-4-yl)pyridin-3-yloxy)cyclohexyloxy)-8-azabicyclo[3.2.1]octane-8-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: di-isopropyl azodicarboxylate; triethylamine; triphenylphosphine / tetrahydrofuran / 18 h / 20 °C / Inert atmosphere

2: trans-bis(triphenylphosphine)palladium dichloride / 1,4-dioxane / 16 h / 110 °C / Inert atmosphere

With trans-bis(triphenylphosphine)palladium dichloride; di-isopropyl azodicarboxylate; triethylamine; triphenylphosphine; In tetrahydrofuran; 1,4-dioxane;

Reference yield:

: 1430746-08-9
(1R,3s,5S)-tert-butyl 3-(4-hydroxyphenoxy)-8-azabicyclo[3.2.1]octane-8-carboxylate

: 1430745-84-8
(1R,3s,5S)-tert-butyl 3-((1r,4R)-4-(2-methyl-6-(pyridazin-4-yl)pyridin-3-yloxy)cyclohexyloxy)-8-azabicyclo[3.2.1]octane-8-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: sodium tetraborate decahydrate; palladium 10% on activated carbon; hydrogen / isopropyl alcohol / 24 h / 80 °C / 9000.9 Torr / Autoclave

2: di-isopropyl azodicarboxylate; triethylamine; triphenylphosphine / tetrahydrofuran / 18 h / 20 °C / Inert atmosphere

3: trans-bis(triphenylphosphine)palladium dichloride / 1,4-dioxane / 16 h / 110 °C / Inert atmosphere

With trans-bis(triphenylphosphine)palladium dichloride; sodium tetraborate decahydrate; di-isopropyl azodicarboxylate; palladium 10% on activated carbon; hydrogen; triethylamine; triphenylphosphine; In tetrahydrofuran; 1,4-dioxane; isopropyl alcohol;