N-(3-chloro-4-fluorophenyl)-6-(3-(5.6-dihydro-[1,2,4]triazolo[4.3-a]pyrazin-7(8H)-yl)propoxy)-7-methoxyquinazolin-4-amine

Base Information

Chemical Name:N-(3-chloro-4-fluorophenyl)-6-(3-(5.6-dihydro-[1,2,4]triazolo[4.3-a]pyrazin-7(8H)-yl)propoxy)-7-methoxyquinazolin-4-amine
CAS No.:1438072-05-9
Molecular Formula:C₂₃H₂₃ClFN₇O₂
Molecular Weight:483.933
Hs Code.:

Synonyms:N-(3-chloro-4-fluorophenyl)-6-(3-(5.6-dihydro-[1,2,4]triazolo[4.3-a]pyrazin-7(8H)-yl)propoxy)-7-methoxyquinazolin-4-amine

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Chemical Property of N-(3-chloro-4-fluorophenyl)-6-(3-(5.6-dihydro-[1,2,4]triazolo[4.3-a]pyrazin-7(8H)-yl)propoxy)-7-methoxyquinazolin-4-amine

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Technology Process of N-(3-chloro-4-fluorophenyl)-6-(3-(5.6-dihydro-[1,2,4]triazolo[4.3-a]pyrazin-7(8H)-yl)propoxy)-7-methoxyquinazolin-4-amine

There total 9 articles about N-(3-chloro-4-fluorophenyl)-6-(3-(5.6-dihydro-[1,2,4]triazolo[4.3-a]pyrazin-7(8H)-yl)propoxy)-7-methoxyquinazolin-4-amine 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: 17.62%

: 912556-91-3
6-(3-chloropropoxy)-N-(3-chloro-4-fluorophenyl)-7-methoxyquinazolin-4-ylamine

: 345311-09-3
5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazine

: 1438072-05-9
N-(3-chloro-4-fluorophenyl)-6-(3-(5.6-dihydro-[1,2,4]triazolo[4.3-a]pyrazin-7(8H)-yl)propoxy)-7-methoxyquinazolin-4-amine

Guidance literature:: With silver carbonate; In N,N-dimethyl-formamide; at 80 ℃; for 36h; Inert atmosphere;

Reference yield:

: 230955-75-6
6-acetoxy-4-chloro-7-methoxyquinazoline

: 1438072-05-9
N-(3-chloro-4-fluorophenyl)-6-(3-(5.6-dihydro-[1,2,4]triazolo[4.3-a]pyrazin-7(8H)-yl)propoxy)-7-methoxyquinazolin-4-amine

Guidance literature:: Multi-step reaction with 4 steps

1: isopropyl alcohol / 5 h / 88 °C

2: water; sodium hydroxide / methanol / 6 h / 20 °C

3: potassium carbonate; potassium iodide / N,N-dimethyl-formamide / 6 h / 40 °C

4: silver carbonate / N,N-dimethyl-formamide / 36 h / 20 - 80 °C / Inert atmosphere

With water; potassium carbonate; silver carbonate; potassium iodide; sodium hydroxide; In methanol; N,N-dimethyl-formamide; isopropyl alcohol;

Reference yield:

: 179688-53-0
6-acetoxy-7-methoxy-3,4-dihydroquinazolin-4-one

: 1438072-05-9
N-(3-chloro-4-fluorophenyl)-6-(3-(5.6-dihydro-[1,2,4]triazolo[4.3-a]pyrazin-7(8H)-yl)propoxy)-7-methoxyquinazolin-4-amine

Guidance literature:: Multi-step reaction with 5 steps

1: thionyl chloride / N,N-dimethyl-formamide / 3 h / 70 °C

2: isopropyl alcohol / 5 h / 88 °C

3: water; sodium hydroxide / methanol / 6 h / 20 °C

4: potassium carbonate; potassium iodide / N,N-dimethyl-formamide / 6 h / 40 °C

5: silver carbonate / N,N-dimethyl-formamide / 36 h / 20 - 80 °C / Inert atmosphere

With thionyl chloride; water; potassium carbonate; silver carbonate; potassium iodide; sodium hydroxide; In methanol; N,N-dimethyl-formamide; isopropyl alcohol;