methyl 4-<2-<<1-<5-chloro-2-(1-piperidinyl)phenyl>2-propyl>amino>-2-oxoethyl>-benzoate

Base Information

Chemical Name:methyl 4-<2-<<1-<5-chloro-2-(1-piperidinyl)phenyl>2-propyl>amino>-2-oxoethyl>-benzoate
CAS No.:83894-80-8
Molecular Formula:C₂₄H₂₉ClN₂O₃
Molecular Weight:428.959
Hs Code.:

Synonyms:methyl 4-<2-<<1-<5-chloro-2-(1-piperidinyl)phenyl>2-propyl>amino>-2-oxoethyl>-benzoate

Suppliers and Price of methyl 4-<2-<<1-<5-chloro-2-(1-piperidinyl)phenyl>2-propyl>amino>-2-oxoethyl>-benzoate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 2 raw suppliers

Chemical Property of methyl 4-<2-<<1-<5-chloro-2-(1-piperidinyl)phenyl>2-propyl>amino>-2-oxoethyl>-benzoate

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of methyl 4-<2-<<1-<5-chloro-2-(1-piperidinyl)phenyl>2-propyl>amino>-2-oxoethyl>-benzoate

There total 7 articles about methyl 4-<2-<<1-<5-chloro-2-(1-piperidinyl)phenyl>2-propyl>amino>-2-oxoethyl>-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: 84.4%

: 83894-80-8
methyl 4-<2-<<1-<5-chloro-2-(1-piperidinyl)phenyl>2-propyl>amino>-2-oxoethyl>-benzoate

Guidance literature:

Reference yield:

: 99-75-2
4-methyl-benzoic acid methyl ester

: 83894-80-8
methyl 4-<2-<<1-<5-chloro-2-(1-piperidinyl)phenyl>2-propyl>amino>-2-oxoethyl>-benzoate

Guidance literature:: Multi-step reaction with 6 steps

1: 80 percent / N-bromosuccinimide, dibenzoyl-peroxide / CCl₄ / 2.5 h / Heating

2: 54 percent / dimethylsulfoxide / 2 h / 40 °C

3: HCl / 8 h / Heating

4: aq. NaHCO₃ / diethyl ether

5: 74 percent / NaOH / methanol / 4 h / 50 °C

6: 1.) N,N'-carbonyldiimidazole / 1.) THF, reflux, 1 h, 2.) THF, RT, overnight

With hydrogenchloride; sodium hydroxide; N-Bromosuccinimide; sodium hydrogencarbonate; 1,1'-carbonyldiimidazole; dibenzoyl peroxide; In methanol; tetrachloromethane; diethyl ether; dimethyl sulfoxide;
DOI:10.1021/jm9810349

Reference yield:

: 2417-72-3
Methyl 4-(bromomethyl)benzoate

: 83894-80-8
methyl 4-<2-<<1-<5-chloro-2-(1-piperidinyl)phenyl>2-propyl>amino>-2-oxoethyl>-benzoate

Guidance literature:: Multi-step reaction with 5 steps

1: 54 percent / dimethylsulfoxide / 2 h / 40 °C

2: HCl / 8 h / Heating

3: aq. NaHCO₃ / diethyl ether

4: 74 percent / NaOH / methanol / 4 h / 50 °C

5: 1.) N,N'-carbonyldiimidazole / 1.) THF, reflux, 1 h, 2.) THF, RT, overnight

With hydrogenchloride; sodium hydroxide; sodium hydrogencarbonate; 1,1'-carbonyldiimidazole; In methanol; diethyl ether; dimethyl sulfoxide;
DOI:10.1021/jm9810349