(2-Chloro-3-methyl-6-nitro-4-piperidin-1-yl-benzylamino)-acetic acid ethyl ester

Base Information

• Chemical Name: (2-Chloro-3-methyl-6-nitro-4-piperidin-1-yl-benzylamino)-acetic acid ethyl ester
• CAS No.: 97113-23-0
• Molecular Formula: C₁₇H₂₄ClN₃O₄
• Molecular Weight: 369.848
• Mol file: 97113-23-0.mol

Synonyms:(2-Chloro-3-methyl-6-nitro-4-piperidin-1-yl-benzylamino)-acetic acid ethyl ester

Chemical Property of (2-Chloro-3-methyl-6-nitro-4-piperidin-1-yl-benzylamino)-acetic acid ethyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (2-Chloro-3-methyl-6-nitro-4-piperidin-1-yl-benzylamino)-acetic acid ethyl ester

There total 7 articles about (2-Chloro-3-methyl-6-nitro-4-piperidin-1-yl-benzylamino)-acetic acid ethyl 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: 46.0%

ethyl bromoacetate (105-36-2) + 5-Methyl-2-nitro-4-piperidin-1-yl-benzylamine (97113-19-4) → (2-Chloro-3-methyl-6-nitro-4-piperidin-1-yl-benzylamino)-acetic acid ethyl ester (97113-23-0)

Guidance literature:

With sodium carbonate; In N,N-dimethyl-formamide;

DOI:10.1021/jm00148a003

Reference yield:

piperidine (110-89-4) → (2-Chloro-3-methyl-6-nitro-4-piperidin-1-yl-benzylamino)-acetic acid ethyl ester (97113-23-0)

Guidance literature:

Multi-step reaction with 3 steps

1: 31 percent / dimethylformamide / 0.5 h / 50 °C

2: 85 percent / CF₃COOH, NaBH₄ / tetrahydrofuran / Ambient temperature

3: 46 percent / Na₂CO₃ / dimethylformamide

With sodium tetrahydroborate; sodium carbonate; trifluoroacetic acid; In tetrahydrofuran; N,N-dimethyl-formamide;

DOI:10.1021/jm00148a003

Reference yield:

N-(4-iodo-3-methylphenyl)acetamide (97113-39-8) → (2-Chloro-3-methyl-6-nitro-4-piperidin-1-yl-benzylamino)-acetic acid ethyl ester (97113-23-0)

Guidance literature:

Multi-step reaction with 6 steps

1: fuming HNO₃ / acetic anhydride / 1 h / Ambient temperature

2: conc. aq. HCl / ethanol / 1.5 h / Heating

3: aq. HCl, NaNO₂ / 1.) acetone, 2.) acetone, water

4: 31 percent / dimethylformamide / 0.5 h / 50 °C

5: 85 percent / CF₃COOH, NaBH₄ / tetrahydrofuran / Ambient temperature

6: 46 percent / Na₂CO₃ / dimethylformamide

With hydrogenchloride; sodium tetrahydroborate; nitric acid; sodium carbonate; trifluoroacetic acid; sodium nitrite; In tetrahydrofuran; ethanol; acetic anhydride; N,N-dimethyl-formamide;

DOI:10.1021/jm00148a003

upstream raw materials:

ethyl bromoacetate

5-Methyl-2-nitro-4-piperidin-1-yl-benzylamine

piperidine

N-(4-iodo-3-methylphenyl)acetamide

Downstream raw materials:

(2-Amino-5-methyl-4-piperidin-1-yl-benzylamino)-acetic acid ethyl ester