phosphoric acid mono-(4-{4-[(2,6-dichloro-benzoylamino)-methyl]-phenyl}-2-oxo-2H-pyridin-1-ylmethyl) ester

Base Information

Chemical Name:phosphoric acid mono-(4-{4-[(2,6-dichloro-benzoylamino)-methyl]-phenyl}-2-oxo-2H-pyridin-1-ylmethyl) ester
CAS No.:1416975-42-2
Molecular Formula:C₂₀H₁₇Cl₂N₂O₆P
Molecular Weight:483.245
Hs Code.:

Synonyms:phosphoric acid mono-(4-{4-[(2,6-dichloro-benzoylamino)-methyl]-phenyl}-2-oxo-2H-pyridin-1-ylmethyl) ester

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Chemical Property of phosphoric acid mono-(4-{4-[(2,6-dichloro-benzoylamino)-methyl]-phenyl}-2-oxo-2H-pyridin-1-ylmethyl) ester

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Technology Process of phosphoric acid mono-(4-{4-[(2,6-dichloro-benzoylamino)-methyl]-phenyl}-2-oxo-2H-pyridin-1-ylmethyl) ester

There total 8 articles about phosphoric acid mono-(4-{4-[(2,6-dichloro-benzoylamino)-methyl]-phenyl}-2-oxo-2H-pyridin-1-ylmethyl) 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:

: 1416975-56-8
phosphoric acid di-tert-butyl ester 4-[4-[(2,6-dichloro-benzoylamino)-methyl]-phenyl]-2-oxo-2H-pyridin-1-ylmethyl ester

: 1416975-42-2
phosphoric acid mono-(4-{4-[(2,6-dichloro-benzoylamino)-methyl]-phenyl}-2-oxo-2H-pyridin-1-ylmethyl) ester

Guidance literature:: With acetic acid; In water; acetonitrile; at 70 ℃; for 4h;

Reference yield:

: 4659-45-4
2,6-Dichlorobenzoyl chloride

: 1416975-42-2
phosphoric acid mono-(4-{4-[(2,6-dichloro-benzoylamino)-methyl]-phenyl}-2-oxo-2H-pyridin-1-ylmethyl) ester

Guidance literature:: Multi-step reaction with 6 steps

1: potassium hydroxide / 20 °C

2: potassium carbonate / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / water; N,N-dimethyl-formamide / 2 h / 70 °C / Inert atmosphere

3: formic acid / dichloromethane / 3 h / 40 °C

4: dichloromethane; N,N-dimethyl-formamide / 5 h / 20 °C

5: tetra-(n-butyl)ammonium iodide; potassium carbonate / N,N-dimethyl-formamide / 4 h / 70 °C

6: acetic acid / water; acetonitrile / 4 h / 70 °C

With formic acid; tetra-(n-butyl)ammonium iodide; potassium carbonate; acetic acid; potassium hydroxide; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In dichloromethane; water; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 1416975-48-8
4-[(2,6-dichloro-benzoylamino)methyl]phenylboronic acid

: 1416975-42-2
phosphoric acid mono-(4-{4-[(2,6-dichloro-benzoylamino)-methyl]-phenyl}-2-oxo-2H-pyridin-1-ylmethyl) ester

Guidance literature:: Multi-step reaction with 5 steps

1: potassium carbonate / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / water; N,N-dimethyl-formamide / 2 h / 70 °C / Inert atmosphere

2: formic acid / dichloromethane / 3 h / 40 °C

3: dichloromethane; N,N-dimethyl-formamide / 5 h / 20 °C

4: tetra-(n-butyl)ammonium iodide; potassium carbonate / N,N-dimethyl-formamide / 4 h / 70 °C

5: acetic acid / water; acetonitrile / 4 h / 70 °C

With formic acid; tetra-(n-butyl)ammonium iodide; potassium carbonate; acetic acid; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In dichloromethane; water; N,N-dimethyl-formamide; acetonitrile;