4-(3'-chloro-4'-fluoroanilino)-6-(hept-6-ynyloxy)-7-methoxyquinazoline

Base Information

Chemical Name:4-(3'-chloro-4'-fluoroanilino)-6-(hept-6-ynyloxy)-7-methoxyquinazoline
CAS No.:1214731-81-3
Molecular Formula:C₂₂H₂₁ClFN₃O₂
Molecular Weight:413.879
Hs Code.:

Synonyms:4-(3'-chloro-4'-fluoroanilino)-6-(hept-6-ynyloxy)-7-methoxyquinazoline

Suppliers and Price of 4-(3'-chloro-4'-fluoroanilino)-6-(hept-6-ynyloxy)-7-methoxyquinazoline

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 4-(3'-chloro-4'-fluoroanilino)-6-(hept-6-ynyloxy)-7-methoxyquinazoline

Chemical Property:

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Technology Process of 4-(3'-chloro-4'-fluoroanilino)-6-(hept-6-ynyloxy)-7-methoxyquinazoline

There total 1 articles about 4-(3'-chloro-4'-fluoroanilino)-6-(hept-6-ynyloxy)-7-methoxyquinazoline 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: 48.0%

: 87462-66-6
1-iodo-6-heptyne

: 184475-71-6
4-(3-chloro-4-fluorophenylamino)-6-hydroxy-7-methoxyquinazoline

: 1214731-81-3
4-(3'-chloro-4'-fluoroanilino)-6-(hept-6-ynyloxy)-7-methoxyquinazoline

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 60 ℃; for 12h; Inert atmosphere;
DOI:10.1016/j.bmc.2009.11.035

Reference yield: 29.0%

: 50-00-0,30525-89-4,61233-19-0
formaldehyd

: 1214731-81-3
4-(3'-chloro-4'-fluoroanilino)-6-(hept-6-ynyloxy)-7-methoxyquinazoline

: 1214731-88-0
4-(3-chloro-4-fluorophenylamino)-6-(octa-6,7-dienyloxy)-7-methoxyquinazoline

Guidance literature:: With diisopropylamine; copper(I) bromide; In 1,4-dioxane; at 110 ℃; for 4h; Inert atmosphere;
DOI:10.1016/j.bmc.2009.11.035