tert-butyl 3-(3-fluoro-4-(methyl(1-methyl-1H-imidazo[4,5-c]pyridin-6-yl)amino)phenyl)azetidine-1-carboxylate

Base Information

Chemical Name:tert-butyl 3-(3-fluoro-4-(methyl(1-methyl-1H-imidazo[4,5-c]pyridin-6-yl)amino)phenyl)azetidine-1-carboxylate
CAS No.:1449669-25-3
Molecular Formula:C₂₂H₂₆FN₅O₂
Molecular Weight:411.479
Hs Code.:

Synonyms:tert-butyl 3-(3-fluoro-4-(methyl(1-methyl-1H-imidazo[4,5-c]pyridin-6-yl)amino)phenyl)azetidine-1-carboxylate

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Chemical Property of tert-butyl 3-(3-fluoro-4-(methyl(1-methyl-1H-imidazo[4,5-c]pyridin-6-yl)amino)phenyl)azetidine-1-carboxylate

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Technology Process of tert-butyl 3-(3-fluoro-4-(methyl(1-methyl-1H-imidazo[4,5-c]pyridin-6-yl)amino)phenyl)azetidine-1-carboxylate

There total 8 articles about tert-butyl 3-(3-fluoro-4-(methyl(1-methyl-1H-imidazo[4,5-c]pyridin-6-yl)amino)phenyl)azetidine-1-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:

: 607373-83-1
2-chloro-4-methoxy-5-nitro-pyridine

: 1449669-25-3
tert-butyl 3-(3-fluoro-4-(methyl(1-methyl-1H-imidazo[4,5-c]pyridin-6-yl)amino)phenyl)azetidine-1-carboxylate

Guidance literature:: Multi-step reaction with 5 steps

1.1: tetrahydrofuran / 2 h / 20 °C

2.1: iron; acetic acid / 1 h / 50 - 80 °C

3.1: 4 h / 100 °C

4.1: caesium carbonate; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl / 1,4-dioxane / 20 h / 110 °C / Inert atmosphere; Sealed tube

5.1: sodium hexamethyldisilazane / tetrahydrofuran; N,N-dimethyl-formamide / 0.5 h / 0 °C

5.2: 2 h / 0 - 20 °C

With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; sodium hexamethyldisilazane; iron; caesium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; acetic acid; In tetrahydrofuran; 1,4-dioxane; N,N-dimethyl-formamide;

Reference yield:

: 1449669-24-2
tert-butyl 3-(3-fluoro-4-(1-methyl-1H-imidazo[4,5-c]pyridin-6-ylamino)phenyl)azetidine-1-carboxylate

: 74-88-4
methyl iodide

: 1449669-25-3
tert-butyl 3-(3-fluoro-4-(methyl(1-methyl-1H-imidazo[4,5-c]pyridin-6-yl)amino)phenyl)azetidine-1-carboxylate

Guidance literature:: tert-butyl 3-(3-fluoro-4-(1-methyl-1H-imidazo[4,5-c]pyridin-6-ylamino)phenyl)azetidine-1-carboxylate; With sodium hexamethyldisilazane; In tetrahydrofuran; N,N-dimethyl-formamide; at 0 ℃; for 0.5h;

methyl iodide; In tetrahydrofuran; N,N-dimethyl-formamide; at 0 - 20 ℃; for 2h;

Reference yield:

: 1449506-71-1
(2-chloro-5-nitro-pyridin-4-yl)-methyl-amine

: 1449669-25-3
tert-butyl 3-(3-fluoro-4-(methyl(1-methyl-1H-imidazo[4,5-c]pyridin-6-yl)amino)phenyl)azetidine-1-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1.1: iron; acetic acid / 1 h / 50 - 80 °C

2.1: 4 h / 100 °C

3.1: caesium carbonate; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl / 1,4-dioxane / 20 h / 110 °C / Inert atmosphere; Sealed tube

4.1: sodium hexamethyldisilazane / tetrahydrofuran; N,N-dimethyl-formamide / 0.5 h / 0 °C

4.2: 2 h / 0 - 20 °C

With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; sodium hexamethyldisilazane; iron; caesium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; acetic acid; In tetrahydrofuran; 1,4-dioxane; N,N-dimethyl-formamide;