1-(4-(6-amino-5-(4-phenoxyphenyl)pyrimidin-4-ylamino)phenyl)pent-3-yn-2-one

Base Information

Chemical Name:1-(4-(6-amino-5-(4-phenoxyphenyl)pyrimidin-4-ylamino)phenyl)pent-3-yn-2-one
CAS No.:1415824-83-7
Molecular Formula:C₂₇H₂₂N₄O₂
Molecular Weight:434.497
Hs Code.:

Synonyms:1-(4-(6-amino-5-(4-phenoxyphenyl)pyrimidin-4-ylamino)phenyl)pent-3-yn-2-one

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Chemical Property of 1-(4-(6-amino-5-(4-phenoxyphenyl)pyrimidin-4-ylamino)phenyl)pent-3-yn-2-one

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Technology Process of 1-(4-(6-amino-5-(4-phenoxyphenyl)pyrimidin-4-ylamino)phenyl)pent-3-yn-2-one

There total 4 articles about 1-(4-(6-amino-5-(4-phenoxyphenyl)pyrimidin-4-ylamino)phenyl)pent-3-yn-2-one 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: 17.0%

: 1415822-58-0
(4-(6-amino-5-(4-phenoxyphenyl)pyrimidin-4-ylamino)phenyl)-N-methoxy-N-methyl-acetamide

: 16466-97-0,13254-27-8
1-propynylmagnesium bromide

: 1415824-83-7
1-(4-(6-amino-5-(4-phenoxyphenyl)pyrimidin-4-ylamino)phenyl)pent-3-yn-2-one

Guidance literature:: In tetrahydrofuran; at 0 - 20 ℃; for 0.5h;

Reference yield:

: 5438-70-0
ethyl (4-amino-3,5-dibromophenyl)acetate

: 1415824-83-7
1-(4-(6-amino-5-(4-phenoxyphenyl)pyrimidin-4-ylamino)phenyl)pent-3-yn-2-one

Guidance literature:: Multi-step reaction with 5 steps

1: N-ethyl-N,N-diisopropylamine / butan-1-ol / 192 h / 115 °C / Inert atmosphere

2: potassium carbonate / palladium diacetate; dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane / 1,4-dioxane; water / 3 h / 150 °C / microwave irradiation; Inert atmosphere

3: sodium hydroxide; water / 1,4-dioxane / 1.5 h / 20 °C

4: N-ethyl-N,N-diisopropylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / N,N-dimethyl-formamide / 20 °C

5: tetrahydrofuran / 0.5 h / 0 - 20 °C

With water; potassium carbonate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; sodium hydroxide; dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane; palladium diacetate; In tetrahydrofuran; 1,4-dioxane; water; N,N-dimethyl-formamide; butan-1-ol; 2: Suzuki Coupling;

Reference yield:

: 1415824-79-1
(4-(6-amino-5-chloro-pyrimidin-4-ylamino)phenyl)acetic acid ethyl ester

: 1415824-83-7
1-(4-(6-amino-5-(4-phenoxyphenyl)pyrimidin-4-ylamino)phenyl)pent-3-yn-2-one

Guidance literature:: Multi-step reaction with 4 steps

1: potassium carbonate / palladium diacetate; dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane / 1,4-dioxane; water / 3 h / 150 °C / microwave irradiation; Inert atmosphere

2: sodium hydroxide; water / 1,4-dioxane / 1.5 h / 20 °C

3: N-ethyl-N,N-diisopropylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / N,N-dimethyl-formamide / 20 °C

4: tetrahydrofuran / 0.5 h / 0 - 20 °C

With water; potassium carbonate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; sodium hydroxide; dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane; palladium diacetate; In tetrahydrofuran; 1,4-dioxane; water; N,N-dimethyl-formamide; 1: Suzuki Coupling;