2-benzyl-6-(4-fluorophenyl)imidazo[2,1-b][1,3,4]thiadiazole-5-carbaldehyde

Base Information

Chemical Name:2-benzyl-6-(4-fluorophenyl)imidazo[2,1-b][1,3,4]thiadiazole-5-carbaldehyde
CAS No.:1175882-77-5
Molecular Formula:C₁₈H₁₂FN₃OS
Molecular Weight:337.377
Hs Code.:

Synonyms:2-benzyl-6-(4-fluorophenyl)imidazo[2,1-b][1,3,4]thiadiazole-5-carbaldehyde

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Chemical Property of 2-benzyl-6-(4-fluorophenyl)imidazo[2,1-b][1,3,4]thiadiazole-5-carbaldehyde

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Technology Process of 2-benzyl-6-(4-fluorophenyl)imidazo[2,1-b][1,3,4]thiadiazole-5-carbaldehyde

There total 5 articles about 2-benzyl-6-(4-fluorophenyl)imidazo[2,1-b][1,3,4]thiadiazole-5-carbaldehyde 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: 55.0%

: 1310578-60-9
2-benzyl-6-(4'-fluorophenyl)-imidazo[2,1-b][1,3,4]thiadiazole

: 68-12-2,33513-42-7
N,N-dimethyl-formamide

: 1175882-77-5
2-benzyl-6-(4-fluorophenyl)imidazo[2,1-b][1,3,4]thiadiazole-5-carbaldehyde

Guidance literature:: N,N-dimethyl-formamide; With trichlorophosphate; at 0 - 5 ℃;

2-benzyl-6-(4'-fluorophenyl)-imidazo[2,1-b][1,3,4]thiadiazole; In N,N-dimethyl-formamide; at 90 ℃; for 8h; Cooling;
DOI:10.1016/j.ejmech.2011.02.064

Reference yield:

: C₉H₁₁N₃S

: 1175882-77-5
2-benzyl-6-(4-fluorophenyl)imidazo[2,1-b][1,3,4]thiadiazole-5-carbaldehyde

Guidance literature:: Multi-step reaction with 2 steps

1.1: ethanol

2.1: trichlorophosphate / 0 - 5 °C

2.2: 8 h / 80 - 90 °C

With trichlorophosphate; In ethanol; 2.1: |Vilsmeier-Haack Formylation / 2.2: |Vilsmeier-Haack Formylation;
DOI:10.1111/febs.13815

Reference yield:

: 403-29-2
2-bromo-4'-fluoroacetophenone

: 1175882-77-5
2-benzyl-6-(4-fluorophenyl)imidazo[2,1-b][1,3,4]thiadiazole-5-carbaldehyde

Guidance literature:: Multi-step reaction with 2 steps

1.1: ethanol / Reflux

1.2: Cooling

2.1: trichlorophosphate / 0 - 5 °C

2.2: 8 h / 90 °C / Cooling

With trichlorophosphate; In ethanol; 2.1: Vilsmeier formylation / 2.2: Vilsmeier formylation;
DOI:10.1016/j.ejmech.2011.02.064