OTAVA-BB 1202440

Base Information

• Chemical Name: OTAVA-BB 1202440
• CAS No.: 329004-08-2
• Molecular Formula: C17H27N3O2
• Molecular Weight: 305.42
• Hs Code.: 2917399590
• Mol file: 329004-08-2.mol

Synonyms:[4-[2-(4-BOC-PIPERAZIN-1-YL)ETHYL]PHENYL]AMINE;OTAVA-BB 1202440;4-(4-aminophenethyl)piperazine-1-carboxylic acid tert-butyl ester;4-[2-(4-Boc-piperazin-1-yl)ethyl]aniline

Chemical Property of OTAVA-BB 1202440

Chemical Property:

• Vapor Pressure: 1.04E-07mmHg at 25°C
• Boiling Point: 433.3°C at 760 mmHg
• Flash Point: 215.9°C
• PSA: 58.80000
• Density: 1.105g/cm³
• LogP: 2.82100

Purity/Quality:

97% ^*data from raw suppliers

4-(4-Aminophenethyl)piperazine-1-carboxylic acid tert-butyl ester ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of OTAVA-BB 1202440

There total 3 articles about OTAVA-BB 1202440 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:

4-[2-(4-nitro-phenyl)-ethyl]-piperazine-1-carboxylic acid tert-butyl ester (130636-60-1) → tert-butyl 4-(4-aminophenethyl)piperazine-1-carboxylate (329004-08-2)

Guidance literature:

With hydrogen; Ra-Ni; In ethanol;

DOI:10.1016/S0960-894X(00)00581-3

Reference yield:

(4-nitrophenyl)ethyl bromide (5339-26-4) → tert-butyl 4-(4-aminophenethyl)piperazine-1-carboxylate (329004-08-2)

Guidance literature:

Multi-step reaction with 2 steps

1: 33 percent / K₂CO₃; NaI / acetonitrile / Heating

2: H₂ / Ra-Ni / ethanol

With hydrogen; potassium carbonate; sodium iodide; Ra-Ni; In ethanol; acetonitrile;

DOI:10.1016/S0960-894X(00)00581-3

Reference yield:

1-t-Butoxycarbonylpiperazine (57260-71-6) → tert-butyl 4-(4-aminophenethyl)piperazine-1-carboxylate (329004-08-2)

Guidance literature:

Multi-step reaction with 2 steps

1: 33 percent / K₂CO₃; NaI / acetonitrile / Heating

2: H₂ / Ra-Ni / ethanol

With hydrogen; potassium carbonate; sodium iodide; Ra-Ni; In ethanol; acetonitrile;

DOI:10.1016/S0960-894X(00)00581-3

upstream raw materials:

4-[2-(4-nitro-phenyl)-ethyl]-piperazine-1-carboxylic acid tert-butyl ester

(4-nitrophenyl)ethyl bromide

1-t-Butoxycarbonylpiperazine

Downstream raw materials:

4-[2-(4-methanesulfonylamino-phenyl)-ethyl]-piperazine-1-carboxylic acid tert-butyl ester

1-[2-(4-methanesulfonamidophenyl)ethyl]piperazine

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