N-hydroxy-4-((1R,4R)-5-m-tolyl-2,5-diazabicyclo[2.2.1]heptan-2-yl)benzamide

Base Information

Chemical Name:N-hydroxy-4-((1R,4R)-5-m-tolyl-2,5-diazabicyclo[2.2.1]heptan-2-yl)benzamide
CAS No.:1024008-03-4
Molecular Formula:C₁₉H₂₁N₃O₂
Molecular Weight:323.395
Hs Code.:

Synonyms:N-hydroxy-4-((1R,4R)-5-m-tolyl-2,5-diazabicyclo[2.2.1]heptan-2-yl)benzamide

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Chemical Property of N-hydroxy-4-((1R,4R)-5-m-tolyl-2,5-diazabicyclo[2.2.1]heptan-2-yl)benzamide

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Technology Process of N-hydroxy-4-((1R,4R)-5-m-tolyl-2,5-diazabicyclo[2.2.1]heptan-2-yl)benzamide

There total 7 articles about N-hydroxy-4-((1R,4R)-5-m-tolyl-2,5-diazabicyclo[2.2.1]heptan-2-yl)benzamide 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: 47.0%

: 1024010-94-3
ethyl 4-((1R,4R)-5-m-tolyl-2,5-diazabicyclo[2.2.1]heptan-2-yl)benzoate

: 1024008-03-4
N-hydroxy-4-((1R,4R)-5-m-tolyl-2,5-diazabicyclo[2.2.1]heptan-2-yl)benzamide

Guidance literature:: With hydroxylamine; potassium hydroxide; In tetrahydrofuran; methanol; water;

Reference yield:

: 61478-27-1
(2S,4S)-N-(tert-butoxycarbonyl)-4-(p-toluenesulfonyloxy)-2-<(p-toluenesulfonyloxy)methyl>pyrrolidine

: 1024008-03-4
N-hydroxy-4-((1R,4R)-5-m-tolyl-2,5-diazabicyclo[2.2.1]heptan-2-yl)benzamide

Guidance literature:: Multi-step reaction with 6 steps

1: toluene / 18 h / 120 °C / Sealed tube

2: hydrogenchloride / 1,4-dioxane

3: dimethyl sulfoxide / 140 °C

4: palladium 10% on activated carbon / methanol / 2 h / Reflux

5: caesium carbonate; bis(tri-t-butylphosphine)palladium ⁽⁰⁾ / tetrahydrofuran / 110 °C / Inert atmosphere

6: hydroxylamine; potassium hydroxide / water; methanol; tetrahydrofuran

With hydrogenchloride; bis(tri-t-butylphosphine)palladium ⁽⁰⁾; palladium 10% on activated carbon; hydroxylamine; caesium carbonate; potassium hydroxide; In tetrahydrofuran; 1,4-dioxane; methanol; water; dimethyl sulfoxide; toluene;

Reference yield:

: 61478-26-0
tert-butyl (2S,4R)-4-hydroxy-2-hydroxymethyl-pyrrolidine-1-carboxylate

: 1024008-03-4
N-hydroxy-4-((1R,4R)-5-m-tolyl-2,5-diazabicyclo[2.2.1]heptan-2-yl)benzamide

Guidance literature:: Multi-step reaction with 7 steps

1: pyridine / 72 h / 0 °C

2: toluene / 18 h / 120 °C / Sealed tube

3: hydrogenchloride / 1,4-dioxane

4: dimethyl sulfoxide / 140 °C

5: palladium 10% on activated carbon / methanol / 2 h / Reflux

6: caesium carbonate; bis(tri-t-butylphosphine)palladium ⁽⁰⁾ / tetrahydrofuran / 110 °C / Inert atmosphere

7: hydroxylamine; potassium hydroxide / water; methanol; tetrahydrofuran

With pyridine; hydrogenchloride; bis(tri-t-butylphosphine)palladium ⁽⁰⁾; palladium 10% on activated carbon; hydroxylamine; caesium carbonate; potassium hydroxide; In tetrahydrofuran; 1,4-dioxane; methanol; water; dimethyl sulfoxide; toluene;