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

Base Information

Chemical Name:(4-{3-[6-(2-tert-butoxycarbonylamino-1-phenylethylamino)pyridin-2-yl]imidazo[1,2-a]pyrazin-8-ylamino}cyclohexyl)carbamic acid tert-butyl ester
CAS No.:1400670-55-4
Molecular Formula:C₃₅H₄₆N₈O₄
Molecular Weight:642.801
Hs Code.:

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

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

There total 10 articles about (4-{3-[6-(2-tert-butoxycarbonylamino-1-phenylethylamino)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:

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

: 174885-99-5
(±)-tert-butyl N-(2-amino-2-phenylethyl)carbamate

: 1400670-55-4
(4-{3-[6-(2-tert-butoxycarbonylamino-1-phenylethylamino)pyridin-2-yl]imidazo[1,2-a]pyrazin-8-ylamino}cyclohexyl)carbamic acid tert-butyl ester

Guidance literature:: With potassium carbonate; DavePhos; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; In 1,4-dioxane; at 135 ℃; for 17h; sealed tube; Inert atmosphere;

Reference yield:

: 67341-07-5
tert-butyl N-(2-hydroxy-2-phenylethyl)carbamate

: 1400670-55-4
(4-{3-[6-(2-tert-butoxycarbonylamino-1-phenylethylamino)pyridin-2-yl]imidazo[1,2-a]pyrazin-8-ylamino}cyclohexyl)carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: triphenylphosphine; diethylazodicarboxylate / 0 - 20 °C

2: hydrazine hydrate / tetrahydrofuran; methanol / 15 h / 65 °C

3: potassium carbonate; DavePhos / tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / 1,4-dioxane / 17 h / 135 °C / sealed tube; Inert atmosphere

With potassium carbonate; hydrazine hydrate; triphenylphosphine; DavePhos; diethylazodicarboxylate; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; In tetrahydrofuran; 1,4-dioxane; methanol;

Reference yield:

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

: 1400670-55-4
(4-{3-[6-(2-tert-butoxycarbonylamino-1-phenylethylamino)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: potassium carbonate; DavePhos / tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / 1,4-dioxane / 17 h / 135 °C / sealed tube; Inert atmosphere

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