(E)-3-(2-(2-tert-butylbenzyl)-1-oxoisoindolin-6-yl)-N-(tetrahydro-2H-pyran-2-yloxy)acrylamide

Base Information

Chemical Name:(E)-3-(2-(2-tert-butylbenzyl)-1-oxoisoindolin-6-yl)-N-(tetrahydro-2H-pyran-2-yloxy)acrylamide
CAS No.:914647-45-3
Molecular Formula:C₂₇H₃₂N₂O₄
Molecular Weight:448.562
Hs Code.:

Synonyms:(E)-3-(2-(2-tert-butylbenzyl)-1-oxoisoindolin-6-yl)-N-(tetrahydro-2H-pyran-2-yloxy)acrylamide

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Chemical Property of (E)-3-(2-(2-tert-butylbenzyl)-1-oxoisoindolin-6-yl)-N-(tetrahydro-2H-pyran-2-yloxy)acrylamide

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Technology Process of (E)-3-(2-(2-tert-butylbenzyl)-1-oxoisoindolin-6-yl)-N-(tetrahydro-2H-pyran-2-yloxy)acrylamide

There total 5 articles about (E)-3-(2-(2-tert-butylbenzyl)-1-oxoisoindolin-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: 95.0%

: 914647-18-0
(E)-3-(2-(2-tert-butylbenzyl)-1-oxoisoindolin-6-yl)acrylic acid

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

: 914647-45-3
(E)-3-(2-(2-tert-butylbenzyl)-1-oxoisoindolin-6-yl)-N-(tetrahydro-2H-pyran-2-yloxy)acrylamide

Guidance literature:: (E)-3-(2-(2-tert-butylbenzyl)-1-oxoisoindolin-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

: 914647-45-3
(E)-3-(2-(2-tert-butylbenzyl)-1-oxoisoindolin-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: 49 percent / triethylamine / methanol / Heating

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

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

4.2: 95 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

: 914647-45-3
(E)-3-(2-(2-tert-butylbenzyl)-1-oxoisoindolin-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: 49 percent / triethylamine / methanol / Heating

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

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

5.2: 95 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