{1-[4-(2-chloro-6-pyridin-2-yl-5-vinyl-pyrrolo[2,3-d]pyrimidin-7-yl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl ester

Base Information

Chemical Name:{1-[4-(2-chloro-6-pyridin-2-yl-5-vinyl-pyrrolo[2,3-d]pyrimidin-7-yl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl ester
CAS No.:1439396-89-0
Molecular Formula:C₂₈H₂₈ClN₅O₂
Molecular Weight:502.016
Hs Code.:

Synonyms:{1-[4-(2-chloro-6-pyridin-2-yl-5-vinyl-pyrrolo[2,3-d]pyrimidin-7-yl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl ester

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Chemical Property of {1-[4-(2-chloro-6-pyridin-2-yl-5-vinyl-pyrrolo[2,3-d]pyrimidin-7-yl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl ester

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Technology Process of {1-[4-(2-chloro-6-pyridin-2-yl-5-vinyl-pyrrolo[2,3-d]pyrimidin-7-yl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl ester

There total 5 articles about {1-[4-(2-chloro-6-pyridin-2-yl-5-vinyl-pyrrolo[2,3-d]pyrimidin-7-yl)-phenyl]-cyclobutyl}-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: 12.0%

: 1439396-87-8
{1-[4-(2-chloro-5-iodo-6-pyridin-2-yl-pyrrolo[2,3-d]pyrimidin-7-yl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl ester

: potassium vinyltrifluoroborate

: 1439396-89-0
{1-[4-(2-chloro-6-pyridin-2-yl-5-vinyl-pyrrolo[2,3-d]pyrimidin-7-yl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl ester

Guidance literature:: With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; triethylamine; In propan-1-ol; at 90 ℃; Inert atmosphere;

Reference yield:

: 1439394-87-2
tert-butyl 1-(4-(2-chloro-5-iodopyrimidin-4-ylamino)phenyl)cyclobutylcarbamate

: 1439396-89-0
{1-[4-(2-chloro-6-pyridin-2-yl-5-vinyl-pyrrolo[2,3-d]pyrimidin-7-yl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; triethylamine / 0.5 h / 80 °C / Inert atmosphere

2: caesium carbonate; bis(tri-t-butylphosphine)palladium⁽⁰⁾; potassium fluoride / 1,4-dioxane / 1 h / 130 °C / Inert atmosphere; Microwave irradiation

3: N-iodo-succinimide / dichloromethane / 20 °C / Inert atmosphere

4: (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; triethylamine / propan-1-ol / 90 °C / Inert atmosphere

With bis-triphenylphosphine-palladium(II) chloride; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium fluoride; N-iodo-succinimide; copper(l) iodide; bis(tri-t-butylphosphine)palladium⁽⁰⁾; caesium carbonate; triethylamine; In 1,4-dioxane; propan-1-ol; dichloromethane;

Reference yield:

: 1439394-88-3
tert-butyl 1-(4-(2-chloro-5-(pyridin-2-ylethynyl)pyrimidin-4-ylamino)phenyl)cyclobutylcarbamate

: 1439396-89-0
{1-[4-(2-chloro-6-pyridin-2-yl-5-vinyl-pyrrolo[2,3-d]pyrimidin-7-yl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: caesium carbonate; bis(tri-t-butylphosphine)palladium⁽⁰⁾; potassium fluoride / 1,4-dioxane / 1 h / 130 °C / Inert atmosphere; Microwave irradiation

2: N-iodo-succinimide / dichloromethane / 20 °C / Inert atmosphere

3: (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; triethylamine / propan-1-ol / 90 °C / Inert atmosphere

With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium fluoride; N-iodo-succinimide; bis(tri-t-butylphosphine)palladium⁽⁰⁾; caesium carbonate; triethylamine; In 1,4-dioxane; propan-1-ol; dichloromethane;