tert-butyl 3-(5-chloro-2-((1s,4s)-4-hydroxycyclohexylamino)pyridin-4-yl)phenyl((tetrahydro-2H-pyran-4-yl)methyl)carbamate

Base Information

Chemical Name:tert-butyl 3-(5-chloro-2-((1s,4s)-4-hydroxycyclohexylamino)pyridin-4-yl)phenyl((tetrahydro-2H-pyran-4-yl)methyl)carbamate
CAS No.:1377698-66-2
Molecular Formula:C₂₈H₃₈ClN₃O₄
Molecular Weight:516.08
Hs Code.:

Synonyms:tert-butyl 3-(5-chloro-2-((1s,4s)-4-hydroxycyclohexylamino)pyridin-4-yl)phenyl((tetrahydro-2H-pyran-4-yl)methyl)carbamate

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Chemical Property of tert-butyl 3-(5-chloro-2-((1s,4s)-4-hydroxycyclohexylamino)pyridin-4-yl)phenyl((tetrahydro-2H-pyran-4-yl)methyl)carbamate

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Technology Process of tert-butyl 3-(5-chloro-2-((1s,4s)-4-hydroxycyclohexylamino)pyridin-4-yl)phenyl((tetrahydro-2H-pyran-4-yl)methyl)carbamate

There total 4 articles about tert-butyl 3-(5-chloro-2-((1s,4s)-4-hydroxycyclohexylamino)pyridin-4-yl)phenyl((tetrahydro-2H-pyran-4-yl)methyl)carbamate 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:

: 1269815-50-0
[3-(5-chloro-2-fluoro-pyridin-4-yl)-phenyl]-(tetrahydro-pyran-4-ylmethyl)-carbamic acid tert-butyl ester

: 56239-26-0
(1s,4s)-4-aminocyclohexan-1-ol hydrochloride

: 1377698-66-2
tert-butyl 3-(5-chloro-2-((1s,4s)-4-hydroxycyclohexylamino)pyridin-4-yl)phenyl((tetrahydro-2H-pyran-4-yl)methyl)carbamate

Guidance literature:: With triethylamine; In dimethyl sulfoxide; at 95 - 100 ℃; for 40h;

Reference yield:

: 659731-48-3
5-chloro-2-fluoro-4-iodopyridine

: 1377698-66-2
tert-butyl 3-(5-chloro-2-((1s,4s)-4-hydroxycyclohexylamino)pyridin-4-yl)phenyl((tetrahydro-2H-pyran-4-yl)methyl)carbamate

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium carbonate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / 1,2-dimethoxyethane / 2 h / 100 °C

2.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.33 h / 0 - 20 °C

2.2: 40 h / 20 - 40 °C

3.1: triethylamine / dimethyl sulfoxide / 40 h / 95 - 100 °C

With sodium hydride; sodium carbonate; triethylamine; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; In 1,2-dimethoxyethane; dimethyl sulfoxide; N,N-dimethyl-formamide; mineral oil;

Reference yield:

: 380430-68-2
3-(tert-butoxycarbonylamino)phenylboronic acid

: 1377698-66-2
tert-butyl 3-(5-chloro-2-((1s,4s)-4-hydroxycyclohexylamino)pyridin-4-yl)phenyl((tetrahydro-2H-pyran-4-yl)methyl)carbamate

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium carbonate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / 1,2-dimethoxyethane / 2 h / 100 °C

2.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.33 h / 0 - 20 °C

2.2: 40 h / 20 - 40 °C

3.1: triethylamine / dimethyl sulfoxide / 40 h / 95 - 100 °C

With sodium hydride; sodium carbonate; triethylamine; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; In 1,2-dimethoxyethane; dimethyl sulfoxide; N,N-dimethyl-formamide; mineral oil;