ethyl 5-(5-{3-isopropoxy-5-[(1-methyl-1H-pyrazol-3-yl)carbamoyl]phenoxy}pyridin-2-yl)-1,2,4-oxadiazole-3-carboxylate

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Chemical Name:ethyl 5-(5-{3-isopropoxy-5-[(1-methyl-1H-pyrazol-3-yl)carbamoyl]phenoxy}pyridin-2-yl)-1,2,4-oxadiazole-3-carboxylate
CAS No.:1310807-56-7
Molecular Formula:C₂₄H₂₄N₆O₆
Molecular Weight:492.491
Hs Code.:

Synonyms:ethyl 5-(5-{3-isopropoxy-5-[(1-methyl-1H-pyrazol-3-yl)carbamoyl]phenoxy}pyridin-2-yl)-1,2,4-oxadiazole-3-carboxylate

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Chemical Property of ethyl 5-(5-{3-isopropoxy-5-[(1-methyl-1H-pyrazol-3-yl)carbamoyl]phenoxy}pyridin-2-yl)-1,2,4-oxadiazole-3-carboxylate

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Technology Process of ethyl 5-(5-{3-isopropoxy-5-[(1-methyl-1H-pyrazol-3-yl)carbamoyl]phenoxy}pyridin-2-yl)-1,2,4-oxadiazole-3-carboxylate

There total 3 articles about ethyl 5-(5-{3-isopropoxy-5-[(1-methyl-1H-pyrazol-3-yl)carbamoyl]phenoxy}pyridin-2-yl)-1,2,4-oxadiazole-3-carboxylate 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:

: 863454-77-7
3-hydroxy-5-[(1-methylethyl)oxy]-N-(1-methyl-1H-pyrazol-3-yl)benzamide

: 1310807-55-6
ethyl 5-(5-fluoropyridin-2-yl)-1,2,4-oxadiazole-3-carboxylate

: 1310807-56-7
ethyl 5-(5-{3-isopropoxy-5-[(1-methyl-1H-pyrazol-3-yl)carbamoyl]phenoxy}pyridin-2-yl)-1,2,4-oxadiazole-3-carboxylate

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 60 - 80 ℃; for 3.5h;

Reference yield:

: 453566-94-4
5-fluoropyridine-2-carboxylic acid hydrochloride

: 1310807-56-7
ethyl 5-(5-{3-isopropoxy-5-[(1-methyl-1H-pyrazol-3-yl)carbamoyl]phenoxy}pyridin-2-yl)-1,2,4-oxadiazole-3-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1: N,N-dimethyl-formamide; oxalyl dichloride / dichloromethane / 1 h

2: dichloromethane / 0.5 h / Cooling with ice

3: toluene-4-sulfonic acid / 1-methyl-pyrrolidin-2-one / 2 h / 130 °C / Cooling with ice

4: potassium carbonate / N,N-dimethyl-formamide / 3.5 h / 60 - 80 °C

With oxalyl dichloride; potassium carbonate; toluene-4-sulfonic acid; N,N-dimethyl-formamide; In 1-methyl-pyrrolidin-2-one; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 717871-83-5
5-fluoropicolinoyl chloride

: 1310807-56-7
ethyl 5-(5-{3-isopropoxy-5-[(1-methyl-1H-pyrazol-3-yl)carbamoyl]phenoxy}pyridin-2-yl)-1,2,4-oxadiazole-3-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: dichloromethane / 0.5 h / Cooling with ice

2: toluene-4-sulfonic acid / 1-methyl-pyrrolidin-2-one / 2 h / 130 °C / Cooling with ice

3: potassium carbonate / N,N-dimethyl-formamide / 3.5 h / 60 - 80 °C

With potassium carbonate; toluene-4-sulfonic acid; In 1-methyl-pyrrolidin-2-one; dichloromethane; N,N-dimethyl-formamide;