(1S,4S)-2,5-diazabicyclo[2.2.1]heptan-2-yl((2R,3aR,6aR)-2-(4-phenylpiperidin-1-yl)octahydropentalen-3a-yl)methanone

Base Information

Chemical Name:(1S,4S)-2,5-diazabicyclo[2.2.1]heptan-2-yl((2R,3aR,6aR)-2-(4-phenylpiperidin-1-yl)octahydropentalen-3a-yl)methanone
CAS No.:1461687-76-2
Molecular Formula:C₂₅H₃₅N₃O
Molecular Weight:393.572
Hs Code.:

Synonyms:(1S,4S)-2,5-diazabicyclo[2.2.1]heptan-2-yl((2R,3aR,6aR)-2-(4-phenylpiperidin-1-yl)octahydropentalen-3a-yl)methanone

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Chemical Property of (1S,4S)-2,5-diazabicyclo[2.2.1]heptan-2-yl((2R,3aR,6aR)-2-(4-phenylpiperidin-1-yl)octahydropentalen-3a-yl)methanone

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Technology Process of (1S,4S)-2,5-diazabicyclo[2.2.1]heptan-2-yl((2R,3aR,6aR)-2-(4-phenylpiperidin-1-yl)octahydropentalen-3a-yl)methanone

There total 11 articles about (1S,4S)-2,5-diazabicyclo[2.2.1]heptan-2-yl((2R,3aR,6aR)-2-(4-phenylpiperidin-1-yl)octahydropentalen-3a-yl)methanone 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:

: 1461687-74-0
(1S,4S)-tert-butyl 5-((2R,3aR,6aR)-2-(4-phenylpiperidin-1-yl)octahydropentalene-3a-carbonyl)-2,5-diazabicyclo[2.2.1]heptane-2-carboxylate

: 1461687-76-2
(1S,4S)-2,5-diazabicyclo[2.2.1]heptan-2-yl((2R,3aR,6aR)-2-(4-phenylpiperidin-1-yl)octahydropentalen-3a-yl)methanone

Guidance literature:: With hydrogenchloride; In 1,4-dioxane; at 0 - 20 ℃; for 1h;

Reference yield:

: 1461687-68-2
(2R,3aR,6aR)-benzyl 2-(4-phenylpiperidin-1-yl)octahydropentalene-3a-carboxylate

: 1461687-76-2
(1S,4S)-2,5-diazabicyclo[2.2.1]heptan-2-yl((2R,3aR,6aR)-2-(4-phenylpiperidin-1-yl)octahydropentalen-3a-yl)methanone

Guidance literature:: Multi-step reaction with 4 steps

1: hydrogen; palladium on activated charcoal / methanol / 1 h / 20 °C / 2585.81 Torr

2: N,N-dimethyl-formamide; oxalyl dichloride / dichloromethane / 0.5 h / 20 °C / Cooling with ice

3: N-ethyl-N,N-diisopropylamine / dichloromethane / 20 °C

4: hydrogenchloride / 1,4-dioxane / 1 h / 0 - 20 °C

With hydrogenchloride; oxalyl dichloride; palladium on activated charcoal; hydrogen; N-ethyl-N,N-diisopropylamine; N,N-dimethyl-formamide; In 1,4-dioxane; methanol; dichloromethane;

Reference yield:

: 1461687-72-8
(2R,3aR,6aR)-2-(4-phenylpiperidin-1-yl)octahydropentalene-3a-carboxylic acid

: 1461687-76-2
(1S,4S)-2,5-diazabicyclo[2.2.1]heptan-2-yl((2R,3aR,6aR)-2-(4-phenylpiperidin-1-yl)octahydropentalen-3a-yl)methanone

Guidance literature:: Multi-step reaction with 3 steps

1: N,N-dimethyl-formamide; oxalyl dichloride / dichloromethane / 0.5 h / 20 °C / Cooling with ice

2: N-ethyl-N,N-diisopropylamine / dichloromethane / 20 °C

3: hydrogenchloride / 1,4-dioxane / 1 h / 0 - 20 °C

With hydrogenchloride; oxalyl dichloride; N-ethyl-N,N-diisopropylamine; N,N-dimethyl-formamide; In 1,4-dioxane; dichloromethane;