3-<3-(3-nitrobenzene-1-carboxamido)benzene-1-carboxamido>propionitrile

Base Information

• Chemical Name: 3-<3-(3-nitrobenzene-1-carboxamido)benzene-1-carboxamido>propionitrile
• CAS No.: 16360-91-1
• Molecular Formula: C₁₇H₁₄N₄O₄
• Molecular Weight: 338.323
• Mol file: 16360-91-1.mol

Synonyms:3-<3-(3-nitrobenzene-1-carboxamido)benzene-1-carboxamido>propionitrile

Chemical Property of 3-<3-(3-nitrobenzene-1-carboxamido)benzene-1-carboxamido>propionitrile

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 3-<3-(3-nitrobenzene-1-carboxamido)benzene-1-carboxamido>propionitrile

There total 7 articles about 3-<3-(3-nitrobenzene-1-carboxamido)benzene-1-carboxamido>propionitrile 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:

3-(3-nitrobenzene-1-carboxamido)propionitrile (16307-87-2) → 3-<3-(3-nitrobenzene-1-carboxamido)benzene-1-carboxamido>propionitrile (16360-91-1)

Guidance literature:

Multi-step reaction with 2 steps

1: H₂ / Raney-Ni / ethanol

2: Py

With pyridine; hydrogen; nickel; In ethanol;

Reference yield:

3-<3-nitrobenzamido>benzoic acid (106590-58-3) → 3-<3-(3-nitrobenzene-1-carboxamido)benzene-1-carboxamido>propionitrile (16360-91-1)

Guidance literature:

Multi-step reaction with 2 steps

1: SOCl₂

2: 4percent aq. NaHCO₃ / acetone / 10 h / Ambient temperature

With thionyl chloride; sodium hydrogencarbonate; In acetone;

Reference yield:

meta-aminobenzoic acid (99-05-8,159139-79-4) → 3-<3-(3-nitrobenzene-1-carboxamido)benzene-1-carboxamido>propionitrile (16360-91-1)

Guidance literature:

Multi-step reaction with 3 steps

1: 88 percent / 4percent aq. NaHCO₃ / acetone / 12 h / Ambient temperature

2: SOCl₂

3: 4percent aq. NaHCO₃ / acetone / 10 h / Ambient temperature

With thionyl chloride; sodium hydrogencarbonate; In acetone;

upstream raw materials:

2-cyanoethylamine

3-<3-nitrobenzamido>benzoyl chloride

3-(3-aminobenzene-1-carboxamido)propionitrile

m-nitrobenzoic acid chloride

Downstream raw materials:

3-(3-<3-(Benzyloxycarbonylaminoacetamido)-benzamido>-benzamido)-propionitril

3''-Amino-3'-benzamido-3-benzamidopropionamidin

3-<3-<3-(3-nitrobenzamido)benzamido>benzamido>benzamidopropionamidine hydrochloride

3-<3-<3-(3-aminobenzamido)benzamido>benzamido>benzamidopropionamidine hydrochloride