methyl 5-(4-(3-chloro-4-fluorophenylamino)-7-(2-methoxyethoxy)quinazolin-6-ylamino)-5-oxopentanoate

Base Information

Chemical Name:methyl 5-(4-(3-chloro-4-fluorophenylamino)-7-(2-methoxyethoxy)quinazolin-6-ylamino)-5-oxopentanoate
CAS No.:1012057-60-1
Molecular Formula:C₂₃H₂₄ClFN₄O₅
Molecular Weight:490.919
Hs Code.:

Synonyms:methyl 5-(4-(3-chloro-4-fluorophenylamino)-7-(2-methoxyethoxy)quinazolin-6-ylamino)-5-oxopentanoate

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Chemical Property of methyl 5-(4-(3-chloro-4-fluorophenylamino)-7-(2-methoxyethoxy)quinazolin-6-ylamino)-5-oxopentanoate

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Technology Process of methyl 5-(4-(3-chloro-4-fluorophenylamino)-7-(2-methoxyethoxy)quinazolin-6-ylamino)-5-oxopentanoate

There total 7 articles about methyl 5-(4-(3-chloro-4-fluorophenylamino)-7-(2-methoxyethoxy)quinazolin-6-ylamino)-5-oxopentanoate 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: 92.0%

N⁴-(3-chloro-4-fluorophenyl)-7-(2-methoxyethoxy)quinazoline-4,6-diamine: 402855-01-0
N⁴-(3-chloro-4-fluorophenyl)-7-(2-methoxyethoxy)quinazoline-4,6-diamine

: 1501-26-4
methyl 4-(chlorocarbonyl)butyrate

: 1012057-60-1
methyl 5-(4-(3-chloro-4-fluorophenylamino)-7-(2-methoxyethoxy)quinazolin-6-ylamino)-5-oxopentanoate

Guidance literature:: With triethylamine; In dichloromethane; at 0 ℃; for 2h;

Reference yield:

: 53449-14-2
7-chloro-6-nitro-4(3H)-quinazolinone

: 1012057-60-1
methyl 5-(4-(3-chloro-4-fluorophenylamino)-7-(2-methoxyethoxy)quinazolin-6-ylamino)-5-oxopentanoate

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium

1.2: 24 h / 90 °C

2.1: trichlorophosphate / 5 h / Heating / reflux

3.1: i-Amyl alcohol / Heating / reflux

4.1: hydrogenchloride; water; iron / ethanol / 2 h / Heating / reflux

4.2: pH 11

5.1: triethylamine / dichloromethane / 2 h / 0 °C

With hydrogenchloride; water; sodium; iron; triethylamine; trichlorophosphate; In ethanol; i-Amyl alcohol; dichloromethane;

Reference yield:

: 31374-18-2
7-chloro-3,4-dihydroquinazolin-4-one

: 1012057-60-1
methyl 5-(4-(3-chloro-4-fluorophenylamino)-7-(2-methoxyethoxy)quinazolin-6-ylamino)-5-oxopentanoate

Guidance literature:: Multi-step reaction with 6 steps

1.1: sulfuric acid; nitric acid / 0 - 45 °C

2.1: sodium

2.2: 24 h / 90 °C

3.1: trichlorophosphate / 5 h / Heating / reflux

4.1: i-Amyl alcohol / Heating / reflux

5.1: hydrogenchloride; water; iron / ethanol / 2 h / Heating / reflux

5.2: pH 11

6.1: triethylamine / dichloromethane / 2 h / 0 °C

With hydrogenchloride; sulfuric acid; water; nitric acid; sodium; iron; triethylamine; trichlorophosphate; In ethanol; i-Amyl alcohol; dichloromethane;