2-[Benzyl-(4-methoxy-benzenesulfonyl)-amino]-N-(tetrahydro-furan-2-ylmethyl)-acetamide

Base Information

• Chemical Name: 2-[Benzyl-(4-methoxy-benzenesulfonyl)-amino]-N-(tetrahydro-furan-2-ylmethyl)-acetamide
• CAS No.: 5741-19-5
• Molecular Formula: C₁₂H₁₈N₂O₄
• Molecular Weight: 254.286
• DSSTox Substance ID: DTXSID60386574
• ChEMBL ID: CHEMBL1906689
• Mol file: 5741-19-5.mol

Synonyms:CBMicro_000865;5741-19-5;Cambridge id 5741195;Oprea1_704022;Oprea1_775115;MLS001219632;CHEMBL1906689;DTXSID60386574;HMS2921E14;SMSF0007732;AKOS000448499;AKOS021999263;CB02146;SMR000611561;BIM-0000827.P001;SR-01000472503;SR-01000472503-1;2-[Benzyl-(4-methoxy-benzenesulfonyl)-amino]-N-(tetrahydro-furan-2-ylmethyl)-acetamide;N~2~-benzyl-N~2~-[(4-methoxyphenyl)sulfonyl]-N~1~-(tetrahydrofuran-2-ylmethyl)glycinamide

Chemical Property of 2-[Benzyl-(4-methoxy-benzenesulfonyl)-amino]-N-(tetrahydro-furan-2-ylmethyl)-acetamide

Chemical Property:

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Density: 1.251g/cm³
• XLogP3: 2.3
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 9
• Exact Mass: 418.15624311
• Heavy Atom Count: 29
• Complexity: 607

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: COC1=CC=C(C=C1)S(=O)(=O)N(CC2=CC=CC=C2)CC(=O)NCC3CCCO3

Technology Process of 2-[Benzyl-(4-methoxy-benzenesulfonyl)-amino]-N-(tetrahydro-furan-2-ylmethyl)-acetamide

There total 2 articles about 2-[Benzyl-(4-methoxy-benzenesulfonyl)-amino]-N-(tetrahydro-furan-2-ylmethyl)-acetamide 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: 90.0%

2-nitrophenyl glycidyl ether (21407-49-8) + isopropylamine (75-31-0) → (+/-)-1-isopropylamino-3-(2-nitrophenoxy)propan-2-ol (5741-19-5)

Guidance literature:

In water; at 20 ℃; for 24h;

DOI:10.1016/j.molcatb.2009.11.004

Reference yield:

→ (+/-)-1-isopropylamino-3-(2-nitrophenoxy)propan-2-ol (5741-19-5)

Guidance literature:

Entspr. Chlorid , Isopropylamin;

upstream raw materials:

2-nitrophenyl glycidyl ether

isopropylamine