N-(3-((5-chloro-2-((4-((diethoxyphosphoryl)methy))amino)phenylamino-4-pyrimidinyl)amino)phenyl)-N-methylbenzamide

Base Information

Chemical Name:N-(3-((5-chloro-2-((4-((diethoxyphosphoryl)methy))amino)phenylamino-4-pyrimidinyl)amino)phenyl)-N-methylbenzamide
CAS No.:1257993-70-6
Molecular Formula:C₂₃H₂₇ClN₅O₄P
Molecular Weight:503.925
Hs Code.:

Synonyms:N-(3-((5-chloro-2-((4-((diethoxyphosphoryl)methy))amino)phenylamino-4-pyrimidinyl)amino)phenyl)-N-methylbenzamide

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Chemical Property of N-(3-((5-chloro-2-((4-((diethoxyphosphoryl)methy))amino)phenylamino-4-pyrimidinyl)amino)phenyl)-N-methylbenzamide

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Technology Process of N-(3-((5-chloro-2-((4-((diethoxyphosphoryl)methy))amino)phenylamino-4-pyrimidinyl)amino)phenyl)-N-methylbenzamide

There total 6 articles about N-(3-((5-chloro-2-((4-((diethoxyphosphoryl)methy))amino)phenylamino-4-pyrimidinyl)amino)phenyl)-N-methylbenzamide 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%

: 761440-08-8
2-[(2,5-dichloropyrimidin-4-yl)amino]-N-methyl-benzamide

: 20074-79-7
diethyl (4-aminobenzyl)phosphonate

: 1257993-70-6
N-(3-((5-chloro-2-((4-((diethoxyphosphoryl)methy))amino)phenylamino-4-pyrimidinyl)amino)phenyl)-N-methylbenzamide

Guidance literature:: With trifluoroacetic acid; In iso-butanol; at 100 ℃; for 12h;
DOI:10.1016/j.bmc.2017.09.041

Reference yield:

: 4141-08-6
2-Amino-N-methylbenzamid

: 1257993-70-6
N-(3-((5-chloro-2-((4-((diethoxyphosphoryl)methy))amino)phenylamino-4-pyrimidinyl)amino)phenyl)-N-methylbenzamide

Guidance literature:: Multi-step reaction with 2 steps

1: N-ethyl-N,N-diisopropylamine / isopropyl alcohol / 6 h / 85 °C

2: trifluoroacetic acid / iso-butanol / 12 h / 100 °C

With N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; In isopropyl alcohol; iso-butanol;
DOI:10.1016/j.bmc.2017.09.041

Reference yield:

: 3400-29-1
N-methyl-2-nitrobenzamide

: 1257993-70-6
N-(3-((5-chloro-2-((4-((diethoxyphosphoryl)methy))amino)phenylamino-4-pyrimidinyl)amino)phenyl)-N-methylbenzamide

Guidance literature:: Multi-step reaction with 3 steps

1: ammonium chloride; iron / methanol; water / 2 h / 70 °C

2: N-ethyl-N,N-diisopropylamine / isopropyl alcohol / 6 h / 85 °C

3: trifluoroacetic acid / iso-butanol / 12 h / 100 °C

With iron; ammonium chloride; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; In methanol; water; isopropyl alcohol; iso-butanol;
DOI:10.1016/j.bmc.2017.09.041