methyl 5-chloro-2-methyl-3-(methyl(tetrahydro-2H-pyran-4-yl)amino)benzoate

Base Information

Chemical Name:methyl 5-chloro-2-methyl-3-(methyl(tetrahydro-2H-pyran-4-yl)amino)benzoate
CAS No.:1403595-51-6
Molecular Formula:C₁₅H₂₀ClNO₃
Molecular Weight:297.782
Hs Code.:

Synonyms:methyl 5-chloro-2-methyl-3-(methyl(tetrahydro-2H-pyran-4-yl)amino)benzoate

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Chemical Property of methyl 5-chloro-2-methyl-3-(methyl(tetrahydro-2H-pyran-4-yl)amino)benzoate

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Technology Process of methyl 5-chloro-2-methyl-3-(methyl(tetrahydro-2H-pyran-4-yl)amino)benzoate

There total 3 articles about methyl 5-chloro-2-methyl-3-(methyl(tetrahydro-2H-pyran-4-yl)amino)benzoate 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: 65.0%

: 1403595-50-5
methyl 5-chloro-2-methyl-3-((tetrahydro-2H-pyran-4-yl)amino)benzoate

: 74-88-4
methyl iodide

: 1403595-51-6
methyl 5-chloro-2-methyl-3-(methyl(tetrahydro-2H-pyran-4-yl)amino)benzoate

Guidance literature:: With caesium carbonate; In acetonitrile; at 80 ℃; for 13h;

Reference yield:

: 7499-06-1
5-chloro-2-methylbenzoic acid

: 1403595-51-6
methyl 5-chloro-2-methyl-3-(methyl(tetrahydro-2H-pyran-4-yl)amino)benzoate

Guidance literature:: Multi-step reaction with 5 steps

1.1: sulfuric acid / 0.17 h / -10 °C

1.2: 0.5 h / -10 °C

2.1: sodium carbonate / N,N-dimethyl-formamide / 4 h / 60 °C

3.1: water; ammonium chloride; iron / ethanol / 1 h / 80 °C

4.1: acetic acid / methanol / 3 h / 20 °C

5.1: caesium carbonate / acetonitrile / 13 h / 80 °C

With sulfuric acid; water; iron; sodium carbonate; ammonium chloride; caesium carbonate; acetic acid; In methanol; ethanol; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 154257-81-5
5-chloro-2-methyl-3-nitrobenzoic acid

: 1403595-51-6
methyl 5-chloro-2-methyl-3-(methyl(tetrahydro-2H-pyran-4-yl)amino)benzoate

Guidance literature:: Multi-step reaction with 4 steps

1: sodium carbonate / N,N-dimethyl-formamide / 4 h / 60 °C

2: water; ammonium chloride; iron / ethanol / 1 h / 80 °C

3: acetic acid / methanol / 3 h / 20 °C

4: caesium carbonate / acetonitrile / 13 h / 80 °C

With water; iron; sodium carbonate; ammonium chloride; caesium carbonate; acetic acid; In methanol; ethanol; N,N-dimethyl-formamide; acetonitrile;