Ethyl (5-(((dimethylamino)methylene)amino)-3-phenyl-2H-pyrido(4,3-b)-1,4-oxazin-7-yl)carbamate

Base Information

Chemical Name:Ethyl (5-(((dimethylamino)methylene)amino)-3-phenyl-2H-pyrido(4,3-b)-1,4-oxazin-7-yl)carbamate
CAS No.:86970-62-9
Molecular Formula:C₁₉H₂₁N₅O₃
Molecular Weight:367.407
Hs Code.:
ChEMBL ID:CHEMBL41059

Synonyms:86970-62-9;Carbamic acid, (5-(((dimethylamino)methylene)amino)-3-phenyl-2H-pyrido(4,3-b)-1,4-oxazin-7-yl)-, ethyl ester;Ethyl (5-(((dimethylamino)methylene)amino)-3-phenyl-2H-pyrido(4,3-b)-1,4-oxazin-7-yl)carbamate;CHEMBL41059;SCHEMBL13327945;Carbamic acid,4-(N,N-dimethylformamidine)-3-phenyl-2H- pyrido[4,3-b][1,4]oxazin-7-yl, ethyl ester;ethyl N-[5-[(E)-dimethylaminomethyleneamino]-3-phenyl-2H-pyrido[4,3-b][1,4]oxazin-7-yl]carbamate

Suppliers and Price of Ethyl (5-(((dimethylamino)methylene)amino)-3-phenyl-2H-pyrido(4,3-b)-1,4-oxazin-7-yl)carbamate

Supply Marketing:

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

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Chemical Property of Ethyl (5-(((dimethylamino)methylene)amino)-3-phenyl-2H-pyrido(4,3-b)-1,4-oxazin-7-yl)carbamate

Chemical Property:

Density:1.266g/cm³
XLogP3:2.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:6
Exact Mass:367.16443955
Heavy Atom Count:27
Complexity:560

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC(=O)NC1=NC(=C2C(=C1)OCC(=N2)C3=CC=CC=C3)N=CN(C)C
Isomeric SMILES:CCOC(=O)NC1=NC(=C2C(=C1)OCC(=N2)C3=CC=CC=C3)/N=C/N(C)C

Technology Process of Ethyl (5-(((dimethylamino)methylene)amino)-3-phenyl-2H-pyrido(4,3-b)-1,4-oxazin-7-yl)carbamate

There total 3 articles about Ethyl (5-(((dimethylamino)methylene)amino)-3-phenyl-2H-pyrido(4,3-b)-1,4-oxazin-7-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: 52.0%

: 4637-24-5
N,N-dimethyl-formamide dimethyl acetal

: 86970-45-8
(5-Amino-3-phenyl-2H-pyrido[4,3-b][1,4]oxazin-7-yl)-carbamic acid ethyl ester; hydrochloride

: 86970-62-9
ethyl <5-<<(dimethylamino)methylene>amino>-3-phenyl-2H-pyrido<4,3-b><1,4>oxazin-7-yl>carbamate

Guidance literature:: In N,N-dimethyl-formamide; for 24h; Ambient temperature;
DOI:10.1021/jm00365a012

Reference yield:

: ethyl (5,6-diamino-4-hydroxypyridin-2-yl)carbamate hydrochloride

: 86970-62-9
ethyl <5-<<(dimethylamino)methylene>amino>-3-phenyl-2H-pyrido<4,3-b><1,4>oxazin-7-yl>carbamate

Guidance literature:: Multi-step reaction with 2 steps

1: 77 percent / potassium acetate, acetic acid / 24 h / Ambient temperature

2: 52 percent / dimethylformamide / 24 h / Ambient temperature

With potassium acetate; acetic acid; In N,N-dimethyl-formamide;
DOI:10.1021/jm00365a012

Reference yield:

: 70-11-1
α-bromoacetophenone

: 86970-62-9
ethyl <5-<<(dimethylamino)methylene>amino>-3-phenyl-2H-pyrido<4,3-b><1,4>oxazin-7-yl>carbamate

Guidance literature:: Multi-step reaction with 2 steps

1: 77 percent / potassium acetate, acetic acid / 24 h / Ambient temperature

2: 52 percent / dimethylformamide / 24 h / Ambient temperature

With potassium acetate; acetic acid; In N,N-dimethyl-formamide;
DOI:10.1021/jm00365a012