4-ETHYLAMINO-PIPERIDINE-1-CARBOXYLIC ACID BENZYL ESTER

Base Information

• Chemical Name: 4-ETHYLAMINO-PIPERIDINE-1-CARBOXYLIC ACID BENZYL ESTER
• CAS No.: 159874-38-1
• Molecular Formula: C15H22N2O2
• Molecular Weight: 262.352
• Hs Code.: 2933399090
• Mol file: 159874-38-1.mol

Synonyms:1-Benzyloxycarbonyl-4-(ethylamino)piperidine;4-Ethylaminopiperidine-1-carboxylic acid benzyl ester;

Chemical Property of 4-ETHYLAMINO-PIPERIDINE-1-CARBOXYLIC ACID BENZYL ESTER

Chemical Property:

• Boiling Point: 388.2±42.0 °C(Predicted)
• PKA: 10.24±0.20(Predicted)
• PSA: 41.57000
• Density: 1.10
• LogP: 2.72590
• Storage Temp.: 2-8°C(protect from light)

Purity/Quality:

97% ^*data from raw suppliers

Benzyl4-(ethylamino)piperidine-1-carboxylate 97% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of 4-ETHYLAMINO-PIPERIDINE-1-CARBOXYLIC ACID BENZYL ESTER

There total 2 articles about 4-ETHYLAMINO-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 4-oxo-1-piperidinecarboxylate (19099-93-5) + ethylamine (75-04-7,85404-22-4) → benzyl 4-(ethylamino)piperidine-1-carboxylate (159874-38-1)

Guidance literature:

benzyl 4-oxo-1-piperidinecarboxylate; ethylamine; With sodium tris(acetoxy)borohydride; acetic acid; In tetrahydrofuran; at 20 ℃; for 68h;

With water; sodium carbonate; In tetrahydrofuran;

Reference yield:

→ benzyl 4-(ethylamino)piperidine-1-carboxylate (159874-38-1)

Guidance literature:

Reference yield: 76.0%

benzyl 4-(ethylamino)piperidine-1-carboxylate (159874-38-1) + methanesulfonyl chloride (124-63-0) → 4-(ethyl-methanesulfonyl-amino)-piperidine-1-carboxylic acid benzyl ester (1131739-50-8)

Guidance literature:

With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃; for 1.33333h;

upstream raw materials:

benzyl 4-oxo-1-piperidinecarboxylate

ethylamine

Downstream raw materials:

tert-butyl 4-{2-[{1-[(benzyloxy)carbonyl]piperidin-4-yl}(ethyl)amino]-2-oxoethyl}piperazine-1-carboxylate

tert-butyl 4-{2-[{1-[(benzyloxy)carbonyl]piperidin-4-yl}(ethyl)amino]-2-oxoethyl}piperidine-1-carboxylate

1-Benzyloxycarbonyl-4-(N-ethylbutyramido)piperidine

1-Benzyloxycarbonyl-4-(N-ethylisobutyramido)piperidine