2-{[6-(4-methoxyphenyl)thieno[3,2-d]pyrimidin-4-yl]thio}-5-phenyl-1,3,4-oxadiazole

Base Information

Chemical Name:2-{[6-(4-methoxyphenyl)thieno[3,2-d]pyrimidin-4-yl]thio}-5-phenyl-1,3,4-oxadiazole
CAS No.:1610730-65-8
Molecular Formula:C₂₁H₁₄N₄O₂S₂
Molecular Weight:418.5
Hs Code.:

Synonyms:2-{[6-(4-methoxyphenyl)thieno[3,2-d]pyrimidin-4-yl]thio}-5-phenyl-1,3,4-oxadiazole

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Chemical Property of 2-{[6-(4-methoxyphenyl)thieno[3,2-d]pyrimidin-4-yl]thio}-5-phenyl-1,3,4-oxadiazole

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Technology Process of 2-{[6-(4-methoxyphenyl)thieno[3,2-d]pyrimidin-4-yl]thio}-5-phenyl-1,3,4-oxadiazole

There total 7 articles about 2-{[6-(4-methoxyphenyl)thieno[3,2-d]pyrimidin-4-yl]thio}-5-phenyl-1,3,4-oxadiazole 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: 57.0%

: 869709-83-1
4-Chloro-6-(4-methoxyphenyl)thieno[3,2-d] pyrimidine

: 3004-42-0
2-Mercapto-5-phenyl-1,3,4-oxadiazole

: 1610730-65-8
2-{[6-(4-methoxyphenyl)thieno[3,2-d]pyrimidin-4-yl]thio}-5-phenyl-1,3,4-oxadiazole

Guidance literature:: With triethylamine; In butan-1-ol; at 100 ℃; for 20h;

Reference yield:

: 14063-79-7
3-chloro-3-(4-methoxyphenyl)acrylaldehyde

: 1610730-65-8
2-{[6-(4-methoxyphenyl)thieno[3,2-d]pyrimidin-4-yl]thio}-5-phenyl-1,3,4-oxadiazole

Guidance literature:: Multi-step reaction with 6 steps

1.1: hydroxylamine hydrochloride / N,N-dimethyl-formamide / 6 h / 60 °C / Inert atmosphere

1.2: 18 h / 130 °C

2.1: sodium hydroxide / ethanol / 15 h / 20 °C

2.2: 2 h / Reflux

3.1: acetic anhydride / 4 h / 20 °C

4.1: ammonium formate / formamide / 6 h / 160 °C / Inert atmosphere

5.1: trichlorophosphate / 2 h / Inert atmosphere; Reflux

6.1: triethylamine / butan-1-ol / 20 h / 100 °C

With hydroxylamine hydrochloride; ammonium formate; triethylamine; sodium hydroxide; trichlorophosphate; In ethanol; acetic anhydride; formamide; N,N-dimethyl-formamide; butan-1-ol;

Reference yield:

: 225385-22-8
6-(4-Methoxyphenyl)thieno[3,2-d] pyrimidin-4(3H)-one

: 1610730-65-8
2-{[6-(4-methoxyphenyl)thieno[3,2-d]pyrimidin-4-yl]thio}-5-phenyl-1,3,4-oxadiazole

Guidance literature:: Multi-step reaction with 2 steps

1: trichlorophosphate / 2 h / Inert atmosphere; Reflux

2: triethylamine / butan-1-ol / 20 h / 100 °C

With triethylamine; trichlorophosphate; In butan-1-ol;