2,2-dimethyl-5-(5-methoxy-2-nitrophenyl)-3-n-pentanoyl-2,3-dihydro-1,3,4-thiadiazole

Base Information

Chemical Name:2,2-dimethyl-5-(5-methoxy-2-nitrophenyl)-3-n-pentanoyl-2,3-dihydro-1,3,4-thiadiazole
CAS No.:1370029-93-8
Molecular Formula:C₁₆H₂₁N₃O₄S
Molecular Weight:351.426
Hs Code.:

Synonyms:2,2-dimethyl-5-(5-methoxy-2-nitrophenyl)-3-n-pentanoyl-2,3-dihydro-1,3,4-thiadiazole

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Chemical Property of 2,2-dimethyl-5-(5-methoxy-2-nitrophenyl)-3-n-pentanoyl-2,3-dihydro-1,3,4-thiadiazole

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Technology Process of 2,2-dimethyl-5-(5-methoxy-2-nitrophenyl)-3-n-pentanoyl-2,3-dihydro-1,3,4-thiadiazole

There total 4 articles about 2,2-dimethyl-5-(5-methoxy-2-nitrophenyl)-3-n-pentanoyl-2,3-dihydro-1,3,4-thiadiazole 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: 70.0%

: C₁₁H₁₃N₃O₃S

: 638-29-9
n-valeryl chloride

: 1370029-93-8
2,2-dimethyl-5-(5-methoxy-2-nitrophenyl)-3-n-pentanoyl-2,3-dihydro-1,3,4-thiadiazole

Guidance literature:: With triethylamine; In dichloromethane; at 20 ℃; for 2h;
DOI:10.1016/j.ejmech.2012.01.047

Reference yield:

: 1370029-89-2
N'-isopropylidene-5-methoxy-2-nitrobenzohydrazide

: 1370029-93-8
2,2-dimethyl-5-(5-methoxy-2-nitrophenyl)-3-n-pentanoyl-2,3-dihydro-1,3,4-thiadiazole

Guidance literature:: Multi-step reaction with 2 steps

1: Lawessons reagent / para-xylene / 5 h / 140 °C / Inert atmosphere

2: triethylamine / dichloromethane / 2 h / 20 °C

With Lawessons reagent; triethylamine; In dichloromethane; para-xylene;
DOI:10.1016/j.ejmech.2012.01.047

Reference yield:

: C₈H₉N₃O₄

: 1370029-93-8
2,2-dimethyl-5-(5-methoxy-2-nitrophenyl)-3-n-pentanoyl-2,3-dihydro-1,3,4-thiadiazole

Guidance literature:: Multi-step reaction with 3 steps

1: ethanol / 2 h / 20 °C / Inert atmosphere

2: Lawessons reagent / para-xylene / 5 h / 140 °C / Inert atmosphere

3: triethylamine / dichloromethane / 2 h / 20 °C

With Lawessons reagent; triethylamine; In ethanol; dichloromethane; para-xylene;
DOI:10.1016/j.ejmech.2012.01.047