acetic acid 3-(3,4-dimethoxy-phenyl)-2-{[2-(1-oxo-4-pyrimidin-5-yl-1H-phthalazin-2-yl)-pyridine-4-carbonyl]-amino}-propyl ester

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Chemical Name:acetic acid 3-(3,4-dimethoxy-phenyl)-2-{[2-(1-oxo-4-pyrimidin-5-yl-1H-phthalazin-2-yl)-pyridine-4-carbonyl]-amino}-propyl ester
CAS No.:209261-95-0
Molecular Formula:C₃₁H₂₈N₆O₆
Molecular Weight:580.6
Hs Code.:

acetic acid 3-(3,4-dimethoxy-phenyl)-2-{[2-(1-oxo-4-pyrimidin-5-yl-1<i>H</i>-phthalazin-2-yl)-pyridine-4-carbonyl]-amino}-propyl ester

Synonyms:acetic acid 3-(3,4-dimethoxy-phenyl)-2-{[2-(1-oxo-4-pyrimidin-5-yl-1H-phthalazin-2-yl)-pyridine-4-carbonyl]-amino}-propyl ester

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Chemical Property of acetic acid 3-(3,4-dimethoxy-phenyl)-2-{[2-(1-oxo-4-pyrimidin-5-yl-1H-phthalazin-2-yl)-pyridine-4-carbonyl]-amino}-propyl ester

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Technology Process of acetic acid 3-(3,4-dimethoxy-phenyl)-2-{[2-(1-oxo-4-pyrimidin-5-yl-1H-phthalazin-2-yl)-pyridine-4-carbonyl]-amino}-propyl ester

There total 5 articles about acetic acid 3-(3,4-dimethoxy-phenyl)-2-{[2-(1-oxo-4-pyrimidin-5-yl-1H-phthalazin-2-yl)-pyridine-4-carbonyl]-amino}-propyl ester 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:

: 66572-56-3
2-bromoisonicotinic acid

: 209261-95-0
acetic acid 3-(3,4-dimethoxy-phenyl)-2-{[2-(1-oxo-4-pyrimidin-5-yl-1H-phthalazin-2-yl)-pyridine-4-carbonyl]-amino}-propyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: DCC; HOBt / CH₂Cl₂ / 25 °C

2: NaBH₄; MeOH / tetrahydrofuran / Heating

3: CuI; K₂CO₃ / dimethylformamide / 120 °C

4: Et₃N / CH₂Cl₂ / 25 °C

With methanol; sodium tetrahydroborate; copper(l) iodide; potassium carbonate; benzotriazol-1-ol; triethylamine; dicyclohexyl-carbodiimide; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; 3: Ullmann condensation;
DOI:10.1016/S0960-894X(03)00438-4

Reference yield:

: 108-24-7
acetic anhydride

: 209261-87-0
N-[2-(3,4-dimethoxy-phenyl)-1-hydroxymethyl-ethyl]-2-(1-oxo-4-pyrimidin-5-yl-1H-phthalazin-2-yl)-isonicotinamide

: 209261-95-0
acetic acid 3-(3,4-dimethoxy-phenyl)-2-{[2-(1-oxo-4-pyrimidin-5-yl-1H-phthalazin-2-yl)-pyridine-4-carbonyl]-amino}-propyl ester

Guidance literature:: With triethylamine; In dichloromethane; at 25 ℃;
DOI:10.1016/S0960-894X(03)00438-4

Reference yield:

: 129077-93-6
(S)-(+)-3,4-dimethoxyphenylalanine ethyl ester hydrochloride

: 209261-95-0
acetic acid 3-(3,4-dimethoxy-phenyl)-2-{[2-(1-oxo-4-pyrimidin-5-yl-1H-phthalazin-2-yl)-pyridine-4-carbonyl]-amino}-propyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: DCC; HOBt / CH₂Cl₂ / 25 °C

2: NaBH₄; MeOH / tetrahydrofuran / Heating

3: CuI; K₂CO₃ / dimethylformamide / 120 °C

4: Et₃N / CH₂Cl₂ / 25 °C

With methanol; sodium tetrahydroborate; copper(l) iodide; potassium carbonate; benzotriazol-1-ol; triethylamine; dicyclohexyl-carbodiimide; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; 3: Ullmann condensation;
DOI:10.1016/S0960-894X(03)00438-4