(E)-3-(1-oxo-2-(1,2-diphenylethyl)isoindolin-6-yl)-N-(tetrahydro-2H-pyran-2-yloxy)acrylamide

Base Information

Chemical Name:(E)-3-(1-oxo-2-(1,2-diphenylethyl)isoindolin-6-yl)-N-(tetrahydro-2H-pyran-2-yloxy)acrylamide
CAS No.:914647-48-6
Molecular Formula:C₃₀H₃₀N₂O₄
Molecular Weight:482.579
Hs Code.:

Synonyms:(E)-3-(1-oxo-2-(1,2-diphenylethyl)isoindolin-6-yl)-N-(tetrahydro-2H-pyran-2-yloxy)acrylamide

Suppliers and Price of (E)-3-(1-oxo-2-(1,2-diphenylethyl)isoindolin-6-yl)-N-(tetrahydro-2H-pyran-2-yloxy)acrylamide

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 (E)-3-(1-oxo-2-(1,2-diphenylethyl)isoindolin-6-yl)-N-(tetrahydro-2H-pyran-2-yloxy)acrylamide

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (E)-3-(1-oxo-2-(1,2-diphenylethyl)isoindolin-6-yl)-N-(tetrahydro-2H-pyran-2-yloxy)acrylamide

There total 6 articles about (E)-3-(1-oxo-2-(1,2-diphenylethyl)isoindolin-6-yl)-N-(tetrahydro-2H-pyran-2-yloxy)acrylamide 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: 99.0%

: 914647-21-5
(E)-3-(1-oxo-2-(1,2-diphenylethyl)isoindolin-6-yl)acrylic acid

: 6723-30-4
O-2-tetrahydro-2H-pyranhydroxylamine

: 914647-48-6
(E)-3-(1-oxo-2-(1,2-diphenylethyl)isoindolin-6-yl)-N-(tetrahydro-2H-pyran-2-yloxy)acrylamide

Guidance literature:: (E)-3-(1-oxo-2-(1,2-diphenylethyl)isoindolin-6-yl)acrylic acid; With chloroformic acid ethyl ester; triethylamine; In tetrahydrofuran; at 0 ℃;

O-2-tetrahydro-2H-pyranhydroxylamine; In tetrahydrofuran; at 20 ℃;
DOI:10.1016/j.bmc.2006.07.008

Reference yield:

: 914646-70-1
methyl 5-(2-(tert-butoxycarbonyl)vinyl)-2-methylbenzoate

: 914647-48-6
(E)-3-(1-oxo-2-(1,2-diphenylethyl)isoindolin-6-yl)-N-(tetrahydro-2H-pyran-2-yloxy)acrylamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: 36 percent / N-bromosuccinimide; benzoyl peroxide / CCl₄ / Heating

2.1: 58 percent / triethylamine / methanol / Heating

3.1: 100 percent / trifluoroacetic acid / CH₂Cl₂ / 20 °C

4.1: ethyl chloroformate; triethylamine / tetrahydrofuran / 0 °C

4.2: 99 percent / tetrahydrofuran / 20 °C

With N-Bromosuccinimide; chloroformic acid ethyl ester; triethylamine; trifluoroacetic acid; dibenzoyl peroxide; In tetrahydrofuran; methanol; tetrachloromethane; dichloromethane;
DOI:10.1016/j.bmc.2006.07.008

Reference yield:

: 914646-68-7
methyl 5-(2-(tert-butoxycarbonyl)-2-bromoethyl)-2-methylbenzoate

: 914647-48-6
(E)-3-(1-oxo-2-(1,2-diphenylethyl)isoindolin-6-yl)-N-(tetrahydro-2H-pyran-2-yloxy)acrylamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: 50 percent / 1,5-diazabicyclo[5.4.0]undec-5-ene / toluene / Heating

2.1: 36 percent / N-bromosuccinimide; benzoyl peroxide / CCl₄ / Heating

3.1: 58 percent / triethylamine / methanol / Heating

4.1: 100 percent / trifluoroacetic acid / CH₂Cl₂ / 20 °C

5.1: ethyl chloroformate; triethylamine / tetrahydrofuran / 0 °C

5.2: 99 percent / tetrahydrofuran / 20 °C

With N-Bromosuccinimide; chloroformic acid ethyl ester; triethylamine; trifluoroacetic acid; 1,5-Diazabicyclo[5.4.0]undec-5-ene; dibenzoyl peroxide; In tetrahydrofuran; methanol; tetrachloromethane; dichloromethane; toluene;
DOI:10.1016/j.bmc.2006.07.008