tert-butyl (6-(4-methoxybenzyl)-4-(2,4-dichlorophenyl)-2-methyl-7-oxo-6,7-dihydro-5H-pyrrolo[3,4-b]pyridin-3-yl)methylcarbamate

Base Information

Chemical Name:tert-butyl (6-(4-methoxybenzyl)-4-(2,4-dichlorophenyl)-2-methyl-7-oxo-6,7-dihydro-5H-pyrrolo[3,4-b]pyridin-3-yl)methylcarbamate
CAS No.:915296-94-5
Molecular Formula:C₂₈H₂₉Cl₂N₃O₄
Molecular Weight:542.462
Hs Code.:

Synonyms:tert-butyl (6-(4-methoxybenzyl)-4-(2,4-dichlorophenyl)-2-methyl-7-oxo-6,7-dihydro-5H-pyrrolo[3,4-b]pyridin-3-yl)methylcarbamate

Suppliers and Price of tert-butyl (6-(4-methoxybenzyl)-4-(2,4-dichlorophenyl)-2-methyl-7-oxo-6,7-dihydro-5H-pyrrolo[3,4-b]pyridin-3-yl)methylcarbamate

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 tert-butyl (6-(4-methoxybenzyl)-4-(2,4-dichlorophenyl)-2-methyl-7-oxo-6,7-dihydro-5H-pyrrolo[3,4-b]pyridin-3-yl)methylcarbamate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of tert-butyl (6-(4-methoxybenzyl)-4-(2,4-dichlorophenyl)-2-methyl-7-oxo-6,7-dihydro-5H-pyrrolo[3,4-b]pyridin-3-yl)methylcarbamate

There total 8 articles about tert-butyl (6-(4-methoxybenzyl)-4-(2,4-dichlorophenyl)-2-methyl-7-oxo-6,7-dihydro-5H-pyrrolo[3,4-b]pyridin-3-yl)methylcarbamate 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: 79.0%

: 6-(4-Methoxybenzyl)-3-(aminomethyl)-4-(2,4-dichlorophenyl)-2-methyl-5,6-dihydropyrrolo[3,4-b]pyridin-7-one

: 691-64-5
di-tert-butyl oxalate

: 915296-94-5
tert-butyl (6-(4-methoxybenzyl)-4-(2,4-dichlorophenyl)-2-methyl-7-oxo-6,7-dihydro-5H-pyrrolo[3,4-b]pyridin-3-yl)methylcarbamate

Guidance literature:: With sodium hydrogencarbonate; In tetrahydrofuran; water; at 20 ℃;

Reference yield:

: 1346242-64-5
C₁₉H₁₅Cl₂NO₃

: 915296-94-5
tert-butyl (6-(4-methoxybenzyl)-4-(2,4-dichlorophenyl)-2-methyl-7-oxo-6,7-dihydro-5H-pyrrolo[3,4-b]pyridin-3-yl)methylcarbamate

Guidance literature:: Multi-step reaction with 6 steps

1: acetic acid / 1.5 h / Reflux

2: nitric acid / 0.5 h / Reflux

3: methanol; lithium borohydride / 15 h / 20 °C

4: methanesulfonyl chloride; triethylamine / dichloromethane / 2 h / 20 °C

5: ammonia / methanol / 0.08 h / 100 °C / Microwave condition

6: sodium hydrogencarbonate / tetrahydrofuran; water / 12 h / 20 °C

With methanol; lithium borohydride; ammonia; nitric acid; sodium hydrogencarbonate; acetic acid; methanesulfonyl chloride; triethylamine; In tetrahydrofuran; methanol; dichloromethane; water;
DOI:10.1016/j.bmcl.2011.09.074

Reference yield:

: 1346242-65-6
C₂₄H₂₀Cl₂N₂O₄

: 915296-94-5
tert-butyl (6-(4-methoxybenzyl)-4-(2,4-dichlorophenyl)-2-methyl-7-oxo-6,7-dihydro-5H-pyrrolo[3,4-b]pyridin-3-yl)methylcarbamate

Guidance literature:: Multi-step reaction with 4 steps

1: methanol; lithium borohydride / 15 h / 20 °C

2: methanesulfonyl chloride; triethylamine / dichloromethane / 2 h / 20 °C

3: ammonia / methanol / 0.08 h / 100 °C / Microwave condition

4: sodium hydrogencarbonate / tetrahydrofuran; water / 12 h / 20 °C

With methanol; lithium borohydride; ammonia; sodium hydrogencarbonate; methanesulfonyl chloride; triethylamine; In tetrahydrofuran; methanol; dichloromethane; water;
DOI:10.1016/j.bmcl.2011.09.074