ethyl N-[6-amino-4-[[(2Z)-2-hydroxyimino-2-naphthalen-2-ylethyl]amino]-5-nitropyridin-2-yl]carbamate

Base Information

Chemical Name:ethyl N-[6-amino-4-[[(2Z)-2-hydroxyimino-2-naphthalen-2-ylethyl]amino]-5-nitropyridin-2-yl]carbamate
CAS No.:83269-19-6
Molecular Formula:C₂₀H₂₀N₆O₅
Molecular Weight:424.416
Hs Code.:
NSC Number:366799
DSSTox Substance ID:DTXSID90430392

Synonyms:NSC366799;83269-19-6;DTXSID90430392;NSC-366799

Suppliers and Price of ethyl N-[6-amino-4-[[(2Z)-2-hydroxyimino-2-naphthalen-2-ylethyl]amino]-5-nitropyridin-2-yl]carbamate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 3 raw suppliers

Chemical Property of ethyl N-[6-amino-4-[[(2Z)-2-hydroxyimino-2-naphthalen-2-ylethyl]amino]-5-nitropyridin-2-yl]carbamate

Chemical Property:

Vapor Pressure:0mmHg at 25°C
Boiling Point:684.757°C at 760 mmHg
Flash Point:367.928°C
Density:1.464g/cm³
XLogP3:4.6
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:9
Rotatable Bond Count:7
Exact Mass:424.14951776
Heavy Atom Count:31
Complexity:657

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC(=O)NC1=NC(=C(C(=C1)NCC(=NO)C2=CC3=CC=CC=C3C=C2)[N+](=O)[O-])N
Isomeric SMILES:CCOC(=O)NC1=NC(=C(C(=C1)NC/C(=N\O)/C2=CC3=CC=CC=C3C=C2)[N+](=O)[O-])N

Technology Process of ethyl N-[6-amino-4-[[(2Z)-2-hydroxyimino-2-naphthalen-2-ylethyl]amino]-5-nitropyridin-2-yl]carbamate

There total 1 articles about ethyl N-[6-amino-4-[[(2Z)-2-hydroxyimino-2-naphthalen-2-ylethyl]amino]-5-nitropyridin-2-yl]carbamate 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: 49.0%

: 6506-86-1
ethyl (6-amino-4-chloro-5-nitropyridin-2-yl)carbamate

: 83269-18-5
aminomethyl 2-naphthyl ketone oxime

: 83269-19-6
ethyl 6-amino-4-<(2-naphthyl-2-oxoethyl)amino>-5-nitro-2-pyridinecarbamate oxime

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In ethanol; for 1h; Heating;
DOI:10.1021/jm00355a018

Reference yield: 66.0%

: 83269-19-6
ethyl 6-amino-4-<(2-naphthyl-2-oxoethyl)amino>-5-nitro-2-pyridinecarbamate oxime

: 83269-06-1
ethyl 6-amino-4-<(2-naphthyl-2-oxoethyl)amino>-5-nitro-2-pyridinecarbamate

Guidance literature:: With hydrogenchloride; In 1,4-dioxane; for 4h; Heating;
DOI:10.1021/jm00355a018

Reference yield:

: 83269-19-6
ethyl 6-amino-4-<(2-naphthyl-2-oxoethyl)amino>-5-nitro-2-pyridinecarbamate oxime

: 83269-07-2
Ethyl 5-amino-1,2-dihydro-3-(2-naphthyl)pyrido[3,4-b]pyrazin-7-ylcarbamate

Guidance literature:: Multi-step reaction with 2 steps

1: 66 percent / 1N HCl / dioxane / 4 h / Heating

2: H₂ / Raney nickel / ethanol / 18 h / 760 Torr / Ambient temperature

With hydrogenchloride; hydrogen; nickel; In 1,4-dioxane; ethanol;
DOI:10.1021/jm00355a018