3-Phenylthiazolo<4',5':4,5>pyrimido<1,6-a>benzimidazole-2,5(3H,4H)-dithione

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Chemical Name:3-Phenylthiazolo<4',5':4,5>pyrimido<1,6-a>benzimidazole-2,5(3H,4H)-dithione
CAS No.:144464-29-9
Molecular Formula:C₁₇H₁₀N₄S₃
Molecular Weight:366.491
Hs Code.:

Synonyms:3-Phenylthiazolo<4',5':4,5>pyrimido<1,6-a>benzimidazole-2,5(3H,4H)-dithione

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Chemical Property of 3-Phenylthiazolo<4',5':4,5>pyrimido<1,6-a>benzimidazole-2,5(3H,4H)-dithione

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Technology Process of 3-Phenylthiazolo<4',5':4,5>pyrimido<1,6-a>benzimidazole-2,5(3H,4H)-dithione

There total 3 articles about 3-Phenylthiazolo<4',5':4,5>pyrimido<1,6-a>benzimidazole-2,5(3H,4H)-dithione 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: 68.0%

: 75-15-0,12122-00-8
carbon disulfide

: 144464-17-5
4-Amino-5-(1H-benzoimidazol-2-yl)-3-phenyl-3H-thiazole-2-thione

: 144464-29-9
3-Phenylthiazolo<4',5':4,5>pyrimido<1,6-a>benzimidazole-2,5(3H,4H)-dithione

Guidance literature:: With potassium hydroxide; In N,N-dimethyl-formamide; for 5h; Ambient temperature;
DOI:10.1002/ardp.19923250908

Reference yield:

: 4414-88-4
1H-benzimidazol-2-acetonitrile

: 144464-29-9
3-Phenylthiazolo<4',5':4,5>pyrimido<1,6-a>benzimidazole-2,5(3H,4H)-dithione

Guidance literature:: Multi-step reaction with 2 steps

1: 79 percent / S, Et₃N / ethanol / 0.5 h / Heating

2: 68 percent / KOH / dimethylformamide / 5 h / Ambient temperature

With potassium hydroxide; triethylamine; In ethanol; N,N-dimethyl-formamide;
DOI:10.1002/ardp.19923250908

Reference yield:

: 103-72-0
phenyl isothiocyanate

: 144464-29-9
3-Phenylthiazolo<4',5':4,5>pyrimido<1,6-a>benzimidazole-2,5(3H,4H)-dithione

Guidance literature:: Multi-step reaction with 2 steps

1: 79 percent / S, Et₃N / ethanol / 0.5 h / Heating

2: 68 percent / KOH / dimethylformamide / 5 h / Ambient temperature

With potassium hydroxide; triethylamine; In ethanol; N,N-dimethyl-formamide;
DOI:10.1002/ardp.19923250908