1-(3-tert-butyl-1-(4-nitrophenyl)-1H-pyrazol-5-yl)-3-(5-(2-morpholinoethoxy)-2H-chromen-8-yl)urea

Base Information

Chemical Name:1-(3-tert-butyl-1-(4-nitrophenyl)-1H-pyrazol-5-yl)-3-(5-(2-morpholinoethoxy)-2H-chromen-8-yl)urea
CAS No.:1071964-53-8
Molecular Formula:C₂₉H₃₄N₆O₆
Molecular Weight:562.626
Hs Code.:

Synonyms:1-(3-tert-butyl-1-(4-nitrophenyl)-1H-pyrazol-5-yl)-3-(5-(2-morpholinoethoxy)-2H-chromen-8-yl)urea

Suppliers and Price of 1-(3-tert-butyl-1-(4-nitrophenyl)-1H-pyrazol-5-yl)-3-(5-(2-morpholinoethoxy)-2H-chromen-8-yl)urea

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 0 raw suppliers

Chemical Property of 1-(3-tert-butyl-1-(4-nitrophenyl)-1H-pyrazol-5-yl)-3-(5-(2-morpholinoethoxy)-2H-chromen-8-yl)urea

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 1-(3-tert-butyl-1-(4-nitrophenyl)-1H-pyrazol-5-yl)-3-(5-(2-morpholinoethoxy)-2H-chromen-8-yl)urea

There total 3 articles about 1-(3-tert-butyl-1-(4-nitrophenyl)-1H-pyrazol-5-yl)-3-(5-(2-morpholinoethoxy)-2H-chromen-8-yl)urea 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: 88.0%

: 1071964-93-6
C₁₅H₂₀N₂O₃

: 1202634-22-7
2,2,2-trichloroethyl (3-(tert-butyl)-1-(4-nitrophenyl)-1H-pyrazol-5-yl)carbamate

: 1071964-53-8
1-(3-tert-butyl-1-(4-nitrophenyl)-1H-pyrazol-5-yl)-3-(5-(2-morpholinoethoxy)-2H-chromen-8-yl)urea

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In dimethyl sulfoxide; at 60 ℃; for 3h;
DOI:10.1080/00397910902883603

Reference yield: 37.0%

: 1071964-93-6
C₁₅H₂₀N₂O₃

: 251658-55-6
3-(tert-butyl)-1-(4-nitrophenyl)-1H-pyrazol-5-amine

: 1071964-53-8
1-(3-tert-butyl-1-(4-nitrophenyl)-1H-pyrazol-5-yl)-3-(5-(2-morpholinoethoxy)-2H-chromen-8-yl)urea

Guidance literature:: With bis(trichloromethyl) carbonate; triethylamine; In dichloromethane; at 25 ℃; for 3h;
DOI:10.3390/molecules19022004

Reference yield:

: 59997-51-2
trimethylacetylacetonitrile

: 636-99-7
4-nitrophenylhydrazine hydrochloride

: 1071964-53-8
1-(3-tert-butyl-1-(4-nitrophenyl)-1H-pyrazol-5-yl)-3-(5-(2-morpholinoethoxy)-2H-chromen-8-yl)urea

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogenchloride / ethanol / 48 h / Reflux

2: triethylamine; bis(trichloromethyl) carbonate / dichloromethane / 3 h / 25 °C

With hydrogenchloride; bis(trichloromethyl) carbonate; triethylamine; In ethanol; dichloromethane;
DOI:10.3390/molecules19022004