6-(4-(benzyloxy)-6-chlorobenzofuran-2-yl)-2-bromoimidazo[2,1-b][1,3,4]thiadiazole

Base Information

Chemical Name:6-(4-(benzyloxy)-6-chlorobenzofuran-2-yl)-2-bromoimidazo[2,1-b][1,3,4]thiadiazole
CAS No.:1476848-23-3
Molecular Formula:C₁₉H₁₁BrClN₃O₂S
Molecular Weight:460.738
Hs Code.:

Synonyms:6-(4-(benzyloxy)-6-chlorobenzofuran-2-yl)-2-bromoimidazo[2,1-b][1,3,4]thiadiazole

Suppliers and Price of 6-(4-(benzyloxy)-6-chlorobenzofuran-2-yl)-2-bromoimidazo[2,1-b][1,3,4]thiadiazole

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 6-(4-(benzyloxy)-6-chlorobenzofuran-2-yl)-2-bromoimidazo[2,1-b][1,3,4]thiadiazole

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 6-(4-(benzyloxy)-6-chlorobenzofuran-2-yl)-2-bromoimidazo[2,1-b][1,3,4]thiadiazole

There total 8 articles about 6-(4-(benzyloxy)-6-chlorobenzofuran-2-yl)-2-bromoimidazo[2,1-b][1,3,4]thiadiazole 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: 73.6%

: 1476848-21-1
1-(4-(benzyloxy)-6-chlorobenzofuran-2-yl)-2-bromoethanone

: 37566-39-5
5-bromo-2-amino-1,3,4-thiadiazole

: 1476848-23-3
6-(4-(benzyloxy)-6-chlorobenzofuran-2-yl)-2-bromoimidazo[2,1-b][1,3,4]thiadiazole

Guidance literature:

Reference yield:

: 1476848-17-5
4-chloro-2,6-dimethoxybenzaldehyde

: 1476848-23-3
6-(4-(benzyloxy)-6-chlorobenzofuran-2-yl)-2-bromoimidazo[2,1-b][1,3,4]thiadiazole

Guidance literature:: Multi-step reaction with 7 steps

1.1: boron tribromide / dichloromethane / 1.17 h / -78 - 20 °C

2.1: caesium carbonate / N,N-dimethyl-formamide / 7 h / 65 °C / Sealed tube

3.1: aluminum (III) chloride / chlorobenzene / 0.67 h / 100 °C / Sealed tube

3.2: 0.5 h / Cooling with ice

4.1: potassium carbonate / N,N-dimethyl-formamide / 1.5 h / 20 °C

5.1: lithium hexamethyldisilazane / tetrahydrofuran / 0.92 h / -78 °C / Inert atmosphere

5.2: 0.92 h / 10 °C / Inert atmosphere

6.1: sodium hydrogencarbonate; N-Bromosuccinimide / tetrahydrofuran / 2.25 h / -30 - 0 °C

7.1: isopropyl alcohol / 7 h / 80 - 150 °C / Microwave irradiation

With aluminum (III) chloride; N-Bromosuccinimide; boron tribromide; sodium hydrogencarbonate; potassium carbonate; caesium carbonate; lithium hexamethyldisilazane; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; chlorobenzene; isopropyl alcohol;

Reference yield:

: 1427396-66-4
4-chloro-2-hydroxy-6-methoxybenzaldehyde

: 1476848-23-3
6-(4-(benzyloxy)-6-chlorobenzofuran-2-yl)-2-bromoimidazo[2,1-b][1,3,4]thiadiazole

Guidance literature:: Multi-step reaction with 6 steps

1.1: caesium carbonate / N,N-dimethyl-formamide / 7 h / 65 °C / Sealed tube

2.1: aluminum (III) chloride / chlorobenzene / 0.67 h / 100 °C / Sealed tube

2.2: 0.5 h / Cooling with ice

3.1: potassium carbonate / N,N-dimethyl-formamide / 1.5 h / 20 °C

4.1: lithium hexamethyldisilazane / tetrahydrofuran / 0.92 h / -78 °C / Inert atmosphere

4.2: 0.92 h / 10 °C / Inert atmosphere

5.1: sodium hydrogencarbonate; N-Bromosuccinimide / tetrahydrofuran / 2.25 h / -30 - 0 °C

6.1: isopropyl alcohol / 7 h / 80 - 150 °C / Microwave irradiation

With aluminum (III) chloride; N-Bromosuccinimide; sodium hydrogencarbonate; potassium carbonate; caesium carbonate; lithium hexamethyldisilazane; In tetrahydrofuran; N,N-dimethyl-formamide; chlorobenzene; isopropyl alcohol;