(2S,4S)-4-(2-{3-[3-(3-cyanophenyl)-6-oxo-6H-pyridazin-1-yl-methyl]phenyl}pyrimidin-5-yloxy)pyrrolidine-2-carboxylic acid

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Chemical Name:(2S,4S)-4-(2-{3-[3-(3-cyanophenyl)-6-oxo-6H-pyridazin-1-yl-methyl]phenyl}pyrimidin-5-yloxy)pyrrolidine-2-carboxylic acid
CAS No.:1233361-02-8
Molecular Formula:C₂₇H₂₂N₆O₄
Molecular Weight:494.509
Hs Code.:

Synonyms:(2S,4S)-4-(2-{3-[3-(3-cyanophenyl)-6-oxo-6H-pyridazin-1-yl-methyl]phenyl}pyrimidin-5-yloxy)pyrrolidine-2-carboxylic acid

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Chemical Property of (2S,4S)-4-(2-{3-[3-(3-cyanophenyl)-6-oxo-6H-pyridazin-1-yl-methyl]phenyl}pyrimidin-5-yloxy)pyrrolidine-2-carboxylic acid

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Technology Process of (2S,4S)-4-(2-{3-[3-(3-cyanophenyl)-6-oxo-6H-pyridazin-1-yl-methyl]phenyl}pyrimidin-5-yloxy)pyrrolidine-2-carboxylic acid

There total 9 articles about (2S,4S)-4-(2-{3-[3-(3-cyanophenyl)-6-oxo-6H-pyridazin-1-yl-methyl]phenyl}pyrimidin-5-yloxy)pyrrolidine-2-carboxylic acid 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:

: 1103506-79-1
3-{1-[3-(5-hydroxy-pyrimidin-2-yl)-benzyl]-6-oxo-1,6-dihydro-pyridazin-3-yl}-benzonitrile

: 74844-91-0
1-tert-butyl 2-methyl (2S,4R)-4-hydroxy-1,2-pyrrolidinedicarboxylate

: 1233361-02-8
(2S,4S)-4-(2-{3-[3-(3-cyanophenyl)-6-oxo-6H-pyridazin-1-yl-methyl]phenyl}pyrimidin-5-yloxy)pyrrolidine-2-carboxylic acid

Guidance literature:: 3-{1-[3-(5-hydroxy-pyrimidin-2-yl)-benzyl]-6-oxo-1,6-dihydro-pyridazin-3-yl}-benzonitrile; 1-tert-butyl 2-methyl (2S,4R)-4-hydroxy-1,2-pyrrolidinedicarboxylate; In 1,4-dioxane; N,N-dimethyl-formamide; at 20 ℃; for 0.25h;

With di-tert-butyl-diazodicarboxylate; In N,N-dimethyl-formamide; at 20 ℃; for 21h;

With hydrogenchloride; In 1,4-dioxane; at 20 ℃; for 15h;

Reference yield:

: 1092568-90-5
(3-(5-bromopyrimidin-2-yl)phenyl)methanol

: 1233361-02-8
(2S,4S)-4-(2-{3-[3-(3-cyanophenyl)-6-oxo-6H-pyridazin-1-yl-methyl]phenyl}pyrimidin-5-yloxy)pyrrolidine-2-carboxylic acid

Guidance literature:: Multi-step reaction with 5 steps

1.1: thionyl chloride / dichloromethane / 3 h / 20 °C

2.1: caesium carbonate / N,N-dimethyl-formamide / 72 h / 40 °C / Inert atmosphere

3.1: potassium acetate / bis-triphenylphosphine-palladium(II) chloride / N,N-dimethyl-formamide / 6 h / 70 °C / Inert atmosphere

4.1: water / tetrahydrofuran / 2 h / 20 °C

5.1: polymer-bound triphenylphosphine / N,N-dimethyl-formamide; 1,4-dioxane / 0.25 h / 20 °C

5.2: 21 h / 20 °C

5.3: 15 h / 20 °C

With thionyl chloride; water; potassium acetate; caesium carbonate; bis-triphenylphosphine-palladium(II) chloride; In tetrahydrofuran; 1,4-dioxane; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 1100598-50-2
5-bromo-2-(3-chloromethyl-phenyl)-pyrimidine

: 1233361-02-8
(2S,4S)-4-(2-{3-[3-(3-cyanophenyl)-6-oxo-6H-pyridazin-1-yl-methyl]phenyl}pyrimidin-5-yloxy)pyrrolidine-2-carboxylic acid

Guidance literature:: Multi-step reaction with 4 steps

1.1: caesium carbonate / N,N-dimethyl-formamide / 72 h / 40 °C / Inert atmosphere

2.1: potassium acetate / bis-triphenylphosphine-palladium(II) chloride / N,N-dimethyl-formamide / 6 h / 70 °C / Inert atmosphere

3.1: water / tetrahydrofuran / 2 h / 20 °C

4.1: polymer-bound triphenylphosphine / N,N-dimethyl-formamide; 1,4-dioxane / 0.25 h / 20 °C

4.2: 21 h / 20 °C

4.3: 15 h / 20 °C

With water; potassium acetate; caesium carbonate; bis-triphenylphosphine-palladium(II) chloride; In tetrahydrofuran; 1,4-dioxane; N,N-dimethyl-formamide;