5,6,7-trimethoxy-2-(4-(5-(4-methoxy-3-nitrophenyl)-1H-imidazol-1-yl)phenyl)benzo[d]thiazole

Base Information

Chemical Name:5,6,7-trimethoxy-2-(4-(5-(4-methoxy-3-nitrophenyl)-1H-imidazol-1-yl)phenyl)benzo[d]thiazole
CAS No.:1393816-16-4
Molecular Formula:C₂₆H₂₂N₄O₆S
Molecular Weight:518.55
Hs Code.:

Synonyms:5,6,7-trimethoxy-2-(4-(5-(4-methoxy-3-nitrophenyl)-1H-imidazol-1-yl)phenyl)benzo[d]thiazole

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Chemical Property of 5,6,7-trimethoxy-2-(4-(5-(4-methoxy-3-nitrophenyl)-1H-imidazol-1-yl)phenyl)benzo[d]thiazole

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Technology Process of 5,6,7-trimethoxy-2-(4-(5-(4-methoxy-3-nitrophenyl)-1H-imidazol-1-yl)phenyl)benzo[d]thiazole

There total 7 articles about 5,6,7-trimethoxy-2-(4-(5-(4-methoxy-3-nitrophenyl)-1H-imidazol-1-yl)phenyl)benzo[d]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:

: 1393816-26-6
C₂₄H₂₁N₃O₆S

: 38622-91-2,36635-61-7
[(p-methylphenyl)sulfonylmethyl]isonitrile

: 1393816-16-4
5,6,7-trimethoxy-2-(4-(5-(4-methoxy-3-nitrophenyl)-1H-imidazol-1-yl)phenyl)benzo[d]thiazole

Guidance literature:: With potassium carbonate; In methanol; 1,2-dimethoxyethane; for 12h; Reflux;

Reference yield:

: 122-04-3
4-nitro-benzoyl chloride

: 1393816-16-4
5,6,7-trimethoxy-2-(4-(5-(4-methoxy-3-nitrophenyl)-1H-imidazol-1-yl)phenyl)benzo[d]thiazole

Guidance literature:: Multi-step reaction with 6 steps

1: pyridine / 3 h / Reflux

2: Lawessons reagent / toluene / 6 h / 110 °C

3: potassium hexacyanoferrate(III); sodium hydroxide / water / 2 h / 90 °C

4: tin(II) chloride dihdyrate / ethanol / 2 h / 80 °C

5: acetic acid / ethanol / 2 h / Reflux

6: potassium carbonate / 1,2-dimethoxyethane; methanol / 12 h / Reflux

With Lawessons reagent; pyridine; tin(II) chloride dihdyrate; potassium carbonate; sodium hydroxide; potassium hexacyanoferrate(III); acetic acid; In methanol; 1,2-dimethoxyethane; ethanol; water; toluene;

Reference yield:

: 24313-88-0
3,4,5-Trimethoxyaniline

: 1393816-16-4
5,6,7-trimethoxy-2-(4-(5-(4-methoxy-3-nitrophenyl)-1H-imidazol-1-yl)phenyl)benzo[d]thiazole

Guidance literature:: Multi-step reaction with 6 steps

1: pyridine / 3 h / Reflux

2: Lawessons reagent / toluene / 6 h / 110 °C

3: potassium hexacyanoferrate(III); sodium hydroxide / water / 2 h / 90 °C

4: tin(II) chloride dihdyrate / ethanol / 2 h / 80 °C

5: acetic acid / ethanol / 2 h / Reflux

6: potassium carbonate / 1,2-dimethoxyethane; methanol / 12 h / Reflux

With Lawessons reagent; pyridine; tin(II) chloride dihdyrate; potassium carbonate; sodium hydroxide; potassium hexacyanoferrate(III); acetic acid; In methanol; 1,2-dimethoxyethane; ethanol; water; toluene;