{4-[(Furan-2-carbonyl)-amino]-phenyl}-[(Z)-tetrahydro-pyran-2-yloxyimino]-acetic acid methyl ester

Base Information

Chemical Name:{4-[(Furan-2-carbonyl)-amino]-phenyl}-[(Z)-tetrahydro-pyran-2-yloxyimino]-acetic acid methyl ester
CAS No.:75626-61-8
Molecular Formula:C₁₉H₂₀N₂O₆
Molecular Weight:372.378
Hs Code.:

Synonyms:{4-[(Furan-2-carbonyl)-amino]-phenyl}-[(Z)-tetrahydro-pyran-2-yloxyimino]-acetic acid methyl ester

Suppliers and Price of {4-[(Furan-2-carbonyl)-amino]-phenyl}-[(Z)-tetrahydro-pyran-2-yloxyimino]-acetic acid methyl ester

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 {4-[(Furan-2-carbonyl)-amino]-phenyl}-[(Z)-tetrahydro-pyran-2-yloxyimino]-acetic acid methyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of {4-[(Furan-2-carbonyl)-amino]-phenyl}-[(Z)-tetrahydro-pyran-2-yloxyimino]-acetic acid methyl ester

There total 9 articles about {4-[(Furan-2-carbonyl)-amino]-phenyl}-[(Z)-tetrahydro-pyran-2-yloxyimino]-acetic acid methyl ester 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: 62.0%

: 527-69-5
2-furancarbonyl chloride

: 75626-60-7
(Z)-methyl 4-amino-α-<<(tetrahydro-2H-pyran-2-yl)-oxy>imino>phenylacetate

: 75626-61-8
{4-[(Furan-2-carbonyl)-amino]-phenyl}-[(Z)-tetrahydro-pyran-2-yloxyimino]-acetic acid methyl ester

Guidance literature:: With triethylamine; In dichloromethane; at 0 ℃; for 0.5h;
DOI:10.1021/jo00314a029

Reference yield:

: 72531-10-3
4-<<(benzyloxy)carbonyl>amino>acetophenone

: 75626-61-8
{4-[(Furan-2-carbonyl)-amino]-phenyl}-[(Z)-tetrahydro-pyran-2-yloxyimino]-acetic acid methyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 75 percent / selenium dioxide / 3 h / 100 °C

2: 59 percent / pyridine / 4 h / 0 °C

3: 98 percent / methanol; diethyl ether / 0 °C

4: 100 percent / H₂ / palladium on carbon / ethyl acetate / 0.5 h

5: 62 percent / triethylamine / CH₂Cl₂ / 0.5 h / 0 °C

With selenium(IV) oxide; hydrogen; triethylamine; palladium on activated charcoal; In pyridine; methanol; diethyl ether; dichloromethane; ethyl acetate;
DOI:10.1021/jo00314a029

Reference yield:

: 75626-51-6
4-<<(benzyloxy)carbonyl>amino>-α-oxophenylacetic acid

: 75626-61-8
{4-[(Furan-2-carbonyl)-amino]-phenyl}-[(Z)-tetrahydro-pyran-2-yloxyimino]-acetic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 59 percent / pyridine / 4 h / 0 °C

2: 98 percent / methanol; diethyl ether / 0 °C

3: 100 percent / H₂ / palladium on carbon / ethyl acetate / 0.5 h

4: 62 percent / triethylamine / CH₂Cl₂ / 0.5 h / 0 °C

With hydrogen; triethylamine; palladium on activated charcoal; In pyridine; methanol; diethyl ether; dichloromethane; ethyl acetate;
DOI:10.1021/jo00314a029