N-(2-aminoethyl)-4-methoxybenzamide

Base Information

• Chemical Name: N-(2-aminoethyl)-4-methoxybenzamide
• CAS No.: 65136-87-0
• Molecular Formula: C10H14N2O2
• Molecular Weight: 194.233
• DSSTox Substance ID: DTXSID60402844
• Nikkaji Number: J983.543A
• Wikidata: Q82206354
• Mol file: 65136-87-0.mol

Synonyms:N-(2-aminoethyl)-4-methoxybenzamide;65136-87-0;SCHEMBL7207554;DTXSID60402844;MVDTXHHGMXWCRJ-UHFFFAOYSA-N;STL194215;AKOS000138821;{N}-(2-aminoethyl)-4-methoxybenzamide;FT-0727400;EN300-45226;F1967-0180

Chemical Property of N-(2-aminoethyl)-4-methoxybenzamide

Chemical Property:

• PSA: 64.35000
• LogP: 1.47490
• XLogP3: 0
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 4
• Exact Mass: 194.105527694
• Heavy Atom Count: 14
• Complexity: 177

Purity/Quality:

99% ^*data from raw suppliers

N-(2-aminoethyl)-4-methoxybenzamide ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: COC1=CC=C(C=C1)C(=O)NCCN

Technology Process of N-(2-aminoethyl)-4-methoxybenzamide

There total 13 articles about N-(2-aminoethyl)-4-methoxybenzamide 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: 83.0%

1-(4-methoxybenzoyl)-1H-1,2,3-benzotriazole (4231-69-0) + ethylenediamine (107-15-3,85404-18-8) → N?(2?aminoethyl)?4?methoxybenzamide (65136-87-0)

Guidance literature:

In butan-1-ol; at 25 ℃; for 3h;

DOI:10.1007/s00706-020-02579-5

Reference yield: 70.0%

N-tert-butoxycarbonyl-N'-(4-methoxybenzoyl)ethylenediamine (1227301-63-4) → N?(2?aminoethyl)?4?methoxybenzamide (65136-87-0)

Guidance literature:

With hydrogenchloride; In 1,4-dioxane; at 20 ℃; for 2h;

DOI:10.1039/c6ob00615a

Reference yield: 38.0%

4-methoxy-benzoyl chloride (100-07-2) + ethylenediamine (107-15-3,85404-18-8) → N?(2?aminoethyl)?4?methoxybenzamide (65136-87-0)

Guidance literature:

In dichloromethane; cooling;

DOI:10.1016/j.bmc.2005.05.069

upstream raw materials:

methyl 4-methoxybenzoate

ethylenediamine

p-methoxybenzoyl fluoride

ethylenediamine hydrochloride

Downstream raw materials:

1β-oxo-6β-(2-phenyl-acetylamino)-1λ⁴-penicillanic acid 2-(4-methoxy-benzoylamino)-ethylamide

N-[2-(4-methoxybenzoylamino)ethyl]-3,4-dimethoxy-5-nitrobenzamide

N-(2-((4-(6-(4-fluorophenyl)imidazo[2,1-b]thiazol-5-yl)pyrimidin-2-yl)amino)ethyl)-4-methoxybenzamide

N-(2-diethylamino-2-methyl-ethyl)-4-methoxy-benzamide

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