4-(4-chlorobutyl)piperidine-1-carboxylic acid benzyl ester

Base Information

• Chemical Name: 4-(4-chlorobutyl)piperidine-1-carboxylic acid benzyl ester
• CAS No.: 464175-15-3
• Molecular Formula: C₁₇H₂₄ClNO₂
• Molecular Weight: 309.836
• Mol file: 464175-15-3.mol

Synonyms:4-(4-chlorobutyl)piperidine-1-carboxylic acid benzyl ester

Chemical Property of 4-(4-chlorobutyl)piperidine-1-carboxylic acid benzyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 4-(4-chlorobutyl)piperidine-1-carboxylic acid benzyl ester

There total 1 articles about 4-(4-chlorobutyl)piperidine-1-carboxylic acid benzyl 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:

benzyl chloroformate (501-53-1,94274-21-2) + 4-(4-chloro-butyl)-piperidine (464175-13-1) → 4-(4-chlorobutyl)piperidine-1-carboxylic acid benzyl ester (464175-15-3)

Guidance literature:

With pyridine; In acetonitrile; at 0 - 20 ℃;

DOI:10.1006/bioo.2001.1227

Reference yield: 82.0%

Boc-Tyr-OH (3978-80-1) + 4-(4-chlorobutyl)piperidine-1-carboxylic acid benzyl ester (464175-15-3) → 4-{4-[4-(2-tert-butoxycarbonylamino-2-carboxy-ethyl)-phenoxy]-butyl}-piperidine-1-carboxylic acid benzyl ester (464175-16-4)

Guidance literature:

With sodium hydride; potassium iodide; In N,N-dimethyl-formamide; at 40 - 45 ℃; for 43h;

DOI:10.1006/bioo.2001.1227

Reference yield:

4-(4-chlorobutyl)piperidine-1-carboxylic acid benzyl ester (464175-15-3) → (S)-2-(4-Butylcarbamoyl-benzenesulfonylamino)-3-[4-(4-piperidin-4-yl-butoxy)-phenyl]-propionic acid

Guidance literature:

Multi-step reaction with 6 steps

1: 82 percent / NaH; KI / dimethylformamide / 43 h / 40 - 45 °C

2: 80 percent / 1,3-dicyclohexylcarbodiimide; 4-dimethylaminopyridine / CH₂Cl₂ / 0 - 20 °C

3: TFA / CH₂Cl₂ / 1 h / 20 °C

4: 60.7 mg / K₂CO₃ / acetonitrile; H₂O / 0 - 20 °C

5: 99 percent / EDC; HOBt; DMAP / CH₂Cl₂ / 0 - 20 °C

6: 100 percent / hydrogen / 10 percent Pd/C / methanol; dimethylformamide / 1 h / 20 °C

With dmap; hydrogen; sodium hydride; potassium carbonate; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; dicyclohexyl-carbodiimide; trifluoroacetic acid; potassium iodide; palladium on activated charcoal; In methanol; dichloromethane; water; N,N-dimethyl-formamide; acetonitrile;

DOI:10.1006/bioo.2001.1227

upstream raw materials:

benzyl chloroformate

4-(4-chloro-butyl)-piperidine

Downstream raw materials:

4-{4-[4-(2-tert-butoxycarbonylamino-2-carboxy-ethyl)-phenoxy]-butyl}-piperidine-1-carboxylic acid benzyl ester

4-{4-[4-((S)-2-Amino-2-benzyloxycarbonyl-ethyl)-phenoxy]-butyl}-piperidine-1-carboxylic acid benzyl ester

4-{4-[4-(2-benzyloxycarbonyl-2-tert-butoxycarbonylamino-ethyl)-phenoxy]-butyl}-piperidine-1-carboxylic acid benzyl ester

4-(4-{4-[(S)-2-Benzyloxycarbonyl-2-(4-carboxy-benzenesulfonylamino)-ethyl]-phenoxy}-butyl)-piperidine-1-carboxylic acid benzyl ester