(4-{3-[6-(2-chlorobenzylamino)pyridin-2-yl]imidazo[1,2-a]pyrazin-8-ylamino}cyclohexyl)carbamic acid tert-butyl ester

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Chemical Name:(4-{3-[6-(2-chlorobenzylamino)pyridin-2-yl]imidazo[1,2-a]pyrazin-8-ylamino}cyclohexyl)carbamic acid tert-butyl ester
CAS No.:1400670-60-1
Molecular Formula:C₂₉H₃₄ClN₇O₂
Molecular Weight:548.088
Hs Code.:

Synonyms:(4-{3-[6-(2-chlorobenzylamino)pyridin-2-yl]imidazo[1,2-a]pyrazin-8-ylamino}cyclohexyl)carbamic acid tert-butyl ester

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Chemical Property of (4-{3-[6-(2-chlorobenzylamino)pyridin-2-yl]imidazo[1,2-a]pyrazin-8-ylamino}cyclohexyl)carbamic acid tert-butyl ester

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Technology Process of (4-{3-[6-(2-chlorobenzylamino)pyridin-2-yl]imidazo[1,2-a]pyrazin-8-ylamino}cyclohexyl)carbamic acid tert-butyl ester

There total 6 articles about (4-{3-[6-(2-chlorobenzylamino)pyridin-2-yl]imidazo[1,2-a]pyrazin-8-ylamino}cyclohexyl)carbamic acid tert-butyl ester 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: 83.0%

: 1400670-30-5
{4-[3-(6-bromopyridin-2-yl)imidazo[1,2-a]pyrazin-8-ylamino]cyclohexyl}carbamic acid tert-butyl ester

: 89-97-4
2-CHLOROBENZYLAMINE

: 1400670-60-1
(4-{3-[6-(2-chlorobenzylamino)pyridin-2-yl]imidazo[1,2-a]pyrazin-8-ylamino}cyclohexyl)carbamic acid tert-butyl ester

Guidance literature:: With sodium t-butanolate; DavePhos; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; In 1,4-dioxane; at 110 ℃; Inert atmosphere; sealed tube;

Reference yield:

: 34160-40-2
6-bromo-2-pyridinecarbaldehyde

: 1400670-60-1
(4-{3-[6-(2-chlorobenzylamino)pyridin-2-yl]imidazo[1,2-a]pyrazin-8-ylamino}cyclohexyl)carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: lithium diisopropyl amide / tetrahydrofuran / 1 h / -10 °C

1.2: 12 h / 20 °C

2.1: N-Bromosuccinimide / 0.5 h / 0 °C

3.1: toluene-4-sulfonic acid / acetonitrile; water / Reflux

4.1: potassium carbonate / N,N-dimethyl-formamide / 15 h / 140 °C

5.1: DavePhos; sodium t-butanolate / tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / 1,4-dioxane / 110 °C / Inert atmosphere; sealed tube

With N-Bromosuccinimide; potassium carbonate; toluene-4-sulfonic acid; sodium t-butanolate; DavePhos; lithium diisopropyl amide; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; In tetrahydrofuran; 1,4-dioxane; water; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 177906-48-8
trans-N-Boc-1,4-cyclohexanediamine

: 1400670-60-1
(4-{3-[6-(2-chlorobenzylamino)pyridin-2-yl]imidazo[1,2-a]pyrazin-8-ylamino}cyclohexyl)carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / N,N-dimethyl-formamide / 15 h / 140 °C

2: DavePhos; sodium t-butanolate / tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / 1,4-dioxane / 110 °C / Inert atmosphere; sealed tube

With potassium carbonate; sodium t-butanolate; DavePhos; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; In 1,4-dioxane; N,N-dimethyl-formamide;