4-chloro-3-(4-cyclopropylbenzyl)-1-{6-[(cyclopropylcarbonyl)amino]-6-deoxy-β-D-glucopyranosyl}-1H-indole

Base Information

Chemical Name:4-chloro-3-(4-cyclopropylbenzyl)-1-{6-[(cyclopropylcarbonyl)amino]-6-deoxy-β-D-glucopyranosyl}-1H-indole
CAS No.:1443333-82-1
Molecular Formula:C₂₈H₃₁ClN₂O₅
Molecular Weight:511.018
Hs Code.:

Synonyms:4-chloro-3-(4-cyclopropylbenzyl)-1-{6-[(cyclopropylcarbonyl)amino]-6-deoxy-β-D-glucopyranosyl}-1H-indole

Suppliers and Price of 4-chloro-3-(4-cyclopropylbenzyl)-1-{6-[(cyclopropylcarbonyl)amino]-6-deoxy-β-D-glucopyranosyl}-1H-indole

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-chloro-3-(4-cyclopropylbenzyl)-1-{6-[(cyclopropylcarbonyl)amino]-6-deoxy-β-D-glucopyranosyl}-1H-indole

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 4-chloro-3-(4-cyclopropylbenzyl)-1-{6-[(cyclopropylcarbonyl)amino]-6-deoxy-β-D-glucopyranosyl}-1H-indole

There total 5 articles about 4-chloro-3-(4-cyclopropylbenzyl)-1-{6-[(cyclopropylcarbonyl)amino]-6-deoxy-β-D-glucopyranosyl}-1H-indole 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: 56.0%

: 1443333-08-1
1-(6-amino-6-deoxy-β-D-glucopyranosyl)-4-chloro-3-(4-cyclopropylbenzyl)-1H-indole

: 4023-34-1
cyclopropanecarboxylic acid chloride

: 1443333-82-1
4-chloro-3-(4-cyclopropylbenzyl)-1-{6-[(cyclopropylcarbonyl)amino]-6-deoxy-β-D-glucopyranosyl}-1H-indole

Guidance literature:: With potassium carbonate; In tetrahydrofuran; at 20 ℃; for 2h; Inert atmosphere;
DOI:10.1016/j.bmc.2016.03.058

Reference yield:

: N-indolylglucoside 4-chloro-3-(4-cyclopropylbenzyl)-1-(β-D-glucopyranosyl)-1H-indole

: 1443333-82-1
4-chloro-3-(4-cyclopropylbenzyl)-1-{6-[(cyclopropylcarbonyl)amino]-6-deoxy-β-D-glucopyranosyl}-1H-indole

Guidance literature:: Multi-step reaction with 4 steps

1: pyridine / 3 h / 0 - 20 °C / Inert atmosphere

2: sodium azide / N,N-dimethyl-formamide / 80 °C

3: acetic acid; zinc / tetrahydrofuran / 20 °C / Inert atmosphere

4: potassium carbonate / tetrahydrofuran / 2 h / 20 °C / Inert atmosphere

With pyridine; sodium azide; potassium carbonate; acetic acid; zinc; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2016.03.058

Reference yield:

: C₂₅H₂₈ClNO₇S

: 1443333-82-1
4-chloro-3-(4-cyclopropylbenzyl)-1-{6-[(cyclopropylcarbonyl)amino]-6-deoxy-β-D-glucopyranosyl}-1H-indole

Guidance literature:: Multi-step reaction with 3 steps

1: sodium azide / N,N-dimethyl-formamide / 80 °C

2: acetic acid; zinc / tetrahydrofuran / 20 °C / Inert atmosphere

3: potassium carbonate / tetrahydrofuran / 2 h / 20 °C / Inert atmosphere

With sodium azide; potassium carbonate; acetic acid; zinc; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2016.03.058