2-(sulfamoylphenyl)-4'-(imino-4-pyridyl)-4-(4''-O-β-D-glucosidoxyphenyl)thiazole

Base Information

Chemical Name:2-(sulfamoylphenyl)-4'-(imino-4-pyridyl)-4-(4''-O-β-D-glucosidoxyphenyl)thiazole
CAS No.:1352305-77-1
Molecular Formula:C₂₇H₂₆N₄O₈S₂
Molecular Weight:598.657
Hs Code.:

Synonyms:2-(sulfamoylphenyl)-4'-(imino-4-pyridyl)-4-(4''-O-β-D-glucosidoxyphenyl)thiazole

Suppliers and Price of 2-(sulfamoylphenyl)-4'-(imino-4-pyridyl)-4-(4''-O-β-D-glucosidoxyphenyl)thiazole

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 2-(sulfamoylphenyl)-4'-(imino-4-pyridyl)-4-(4''-O-β-D-glucosidoxyphenyl)thiazole

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Technology Process of 2-(sulfamoylphenyl)-4'-(imino-4-pyridyl)-4-(4''-O-β-D-glucosidoxyphenyl)thiazole

There total 6 articles about 2-(sulfamoylphenyl)-4'-(imino-4-pyridyl)-4-(4''-O-β-D-glucosidoxyphenyl)thiazole 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: 65.0%

: 1352305-71-5
2-(sulfamoylphenyl)-4'-(imino-4-pyridyl)-4-(2,3,4,6-tetra-O-acetyl-4''-O-β-D-glucosidoxyphenyl)thiazole

: 1352305-77-1
2-(sulfamoylphenyl)-4'-(imino-4-pyridyl)-4-(4''-O-β-D-glucosidoxyphenyl)thiazole

Guidance literature:: 2-(sulfamoylphenyl)-4'-(imino-4-pyridyl)-4-(2,3,4,6-tetra-O-acetyl-4''-O-β-D-glucosidoxyphenyl)thiazole; With sodium methylate; In methanol; at 20 ℃; for 24h;

In methanol;
DOI:10.1002/jhet.713

Reference yield:

: 1352305-60-2
2-(4-aminophenylsulfonamido)-4-(4-hydroxyphenyl)thiazole

: 1352305-77-1
2-(sulfamoylphenyl)-4'-(imino-4-pyridyl)-4-(4''-O-β-D-glucosidoxyphenyl)thiazole

Guidance literature:: Multi-step reaction with 3 steps

1.1: sulfuric acid / ethanol / Reflux

2.1: potassium hydroxide / methanol

2.2: 26 h / 0 °C

3.1: sodium methylate / methanol / 24 h / 20 °C

3.2: Amberlite IR-120 (H⁺ form)

With sulfuric acid; sodium methylate; potassium hydroxide; In methanol; ethanol;
DOI:10.1002/jhet.713

Reference yield:

: 1352305-59-9
2-(4-acetamidophenylsulfonamido)-4-(4-hydroxyphenyl)thiazole

: 1352305-77-1
2-(sulfamoylphenyl)-4'-(imino-4-pyridyl)-4-(4''-O-β-D-glucosidoxyphenyl)thiazole

Guidance literature:: Multi-step reaction with 4 steps

1.1: hydrogenchloride / water / 1 h / Reflux

2.1: sulfuric acid / ethanol / Reflux

3.1: potassium hydroxide / methanol

3.2: 26 h / 0 °C

4.1: sodium methylate / methanol / 24 h / 20 °C

4.2: Amberlite IR-120 (H⁺ form)

With hydrogenchloride; sulfuric acid; sodium methylate; potassium hydroxide; In methanol; ethanol; water;
DOI:10.1002/jhet.713