(2-(2-amino-3-((1S,4S)-2-oxa-5-azabicyclo[2.2.1]heptan-5-yl)quinolin-6-yl)-3-methylphenyl)(pyrrolidin-1-yl)methanone

Base Information

Chemical Name:(2-(2-amino-3-((1S,4S)-2-oxa-5-azabicyclo[2.2.1]heptan-5-yl)quinolin-6-yl)-3-methylphenyl)(pyrrolidin-1-yl)methanone
CAS No.:1319194-80-3
Molecular Formula:C₂₆H₂₈N₄O₂
Molecular Weight:428.534
Hs Code.:

Synonyms:(2-(2-amino-3-((1S,4S)-2-oxa-5-azabicyclo[2.2.1]heptan-5-yl)quinolin-6-yl)-3-methylphenyl)(pyrrolidin-1-yl)methanone

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Chemical Property of (2-(2-amino-3-((1S,4S)-2-oxa-5-azabicyclo[2.2.1]heptan-5-yl)quinolin-6-yl)-3-methylphenyl)(pyrrolidin-1-yl)methanone

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Technology Process of (2-(2-amino-3-((1S,4S)-2-oxa-5-azabicyclo[2.2.1]heptan-5-yl)quinolin-6-yl)-3-methylphenyl)(pyrrolidin-1-yl)methanone

There total 8 articles about (2-(2-amino-3-((1S,4S)-2-oxa-5-azabicyclo[2.2.1]heptan-5-yl)quinolin-6-yl)-3-methylphenyl)(pyrrolidin-1-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:

: 1319197-37-9
2-((1S,4S)-2-oxa-5-azabicyclo[2.2.1]heptan-5-yl)acetonitrile

: 1319197-40-4
4-amino-2'-methyl-6'-(pyrrolidine-1-carbonyl)biphenyl-3-carbaldehyde

: 1319194-80-3
(2-(2-amino-3-((1S,4S)-2-oxa-5-azabicyclo[2.2.1]heptan-5-yl)quinolin-6-yl)-3-methylphenyl)(pyrrolidin-1-yl)methanone

Guidance literature:: With potassium hydroxide; In dimethyl sulfoxide; at 80 ℃; for 18.75h;

Reference yield:

: 363185-87-9
methyl 2-amino-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate

: 1319194-80-3
(2-(2-amino-3-((1S,4S)-2-oxa-5-azabicyclo[2.2.1]heptan-5-yl)quinolin-6-yl)-3-methylphenyl)(pyrrolidin-1-yl)methanone

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium phosphate / tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; XPhos / 1,4-dioxane; water / 0.2 h / 140 °C / microwave irradiation

2.1: diisobutylaluminium hydride / dichloromethane; n-heptane / 0.5 h / -78 °C / Inert atmosphere

2.2: -78 - 20 °C / Inert atmosphere

3.1: manganese(IV) oxide / dichloromethane / 0.33 h / 20 °C

4.1: potassium hydroxide / dimethyl sulfoxide / 18.75 h / 80 °C

With manganese(IV) oxide; potassium phosphate; diisobutylaluminium hydride; potassium hydroxide; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; XPhos; In 1,4-dioxane; n-heptane; dichloromethane; water; dimethyl sulfoxide;

Reference yield:

: 53663-39-1
3-methyl-2-bromobenzoic acid

: 1319194-80-3
(2-(2-amino-3-((1S,4S)-2-oxa-5-azabicyclo[2.2.1]heptan-5-yl)quinolin-6-yl)-3-methylphenyl)(pyrrolidin-1-yl)methanone

Guidance literature:: Multi-step reaction with 5 steps

1.1: 1,1'-carbonyldiimidazole / tetrahydrofuran / 14 h / 20 °C

1.2: 8 h

2.1: potassium phosphate / tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; XPhos / 1,4-dioxane; water / 0.2 h / 140 °C / microwave irradiation

3.1: diisobutylaluminium hydride / dichloromethane; n-heptane / 0.5 h / -78 °C / Inert atmosphere

3.2: -78 - 20 °C / Inert atmosphere

4.1: manganese(IV) oxide / dichloromethane / 0.33 h / 20 °C

5.1: potassium hydroxide / dimethyl sulfoxide / 18.75 h / 80 °C

With manganese(IV) oxide; potassium phosphate; diisobutylaluminium hydride; 1,1'-carbonyldiimidazole; potassium hydroxide; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; XPhos; In tetrahydrofuran; 1,4-dioxane; n-heptane; dichloromethane; water; dimethyl sulfoxide;