5-[5-(3-{[(2S)-1-methoxypropan-2-yl]oxy}-5-[(1-methyl-1H-pyrazol-3-yl)carbamoyl]phenoxy)pyridin-2-yl]-N-methyl-1,3,4-oxadiazole-2-carboxamide

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Chemical Name:5-[5-(3-{[(2S)-1-methoxypropan-2-yl]oxy}-5-[(1-methyl-1H-pyrazol-3-yl)carbamoyl]phenoxy)pyridin-2-yl]-N-methyl-1,3,4-oxadiazole-2-carboxamide
CAS No.:1310805-86-7
Molecular Formula:C₂₄H₂₅N₇O₆
Molecular Weight:507.506
Hs Code.:

Synonyms:5-[5-(3-{[(2S)-1-methoxypropan-2-yl]oxy}-5-[(1-methyl-1H-pyrazol-3-yl)carbamoyl]phenoxy)pyridin-2-yl]-N-methyl-1,3,4-oxadiazole-2-carboxamide

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Chemical Property of 5-[5-(3-{[(2S)-1-methoxypropan-2-yl]oxy}-5-[(1-methyl-1H-pyrazol-3-yl)carbamoyl]phenoxy)pyridin-2-yl]-N-methyl-1,3,4-oxadiazole-2-carboxamide

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Technology Process of 5-[5-(3-{[(2S)-1-methoxypropan-2-yl]oxy}-5-[(1-methyl-1H-pyrazol-3-yl)carbamoyl]phenoxy)pyridin-2-yl]-N-methyl-1,3,4-oxadiazole-2-carboxamide

There total 5 articles about 5-[5-(3-{[(2S)-1-methoxypropan-2-yl]oxy}-5-[(1-methyl-1H-pyrazol-3-yl)carbamoyl]phenoxy)pyridin-2-yl]-N-methyl-1,3,4-oxadiazole-2-carboxamide 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:

: 863504-73-8
3-hydroxy-5-{[(1S)-2-methoxy-1-methylethyl]oxy}-N-(1-methyl-1H-pyrazol-3-yl)benzamide

: 1310807-74-9
5-(5-fluoropyridin-2-yl)-N-methyl-1,3,4-oxadiazole-2-carboxamide

: 1310805-86-7
5-[5-(3-{[(2S)-1-methoxypropan-2-yl]oxy}-5-[(1-methyl-1H-pyrazol-3-yl)carbamoyl]phenoxy)pyridin-2-yl]-N-methyl-1,3,4-oxadiazole-2-carboxamide

Guidance literature:: With potassium carbonate; In 1-methyl-pyrrolidin-2-one; at 20 - 110 ℃; for 4h; Inert atmosphere;

Reference yield:

: 107504-08-5
5-fluoropicolinic acid

: 1310805-86-7
5-[5-(3-{[(2S)-1-methoxypropan-2-yl]oxy}-5-[(1-methyl-1H-pyrazol-3-yl)carbamoyl]phenoxy)pyridin-2-yl]-N-methyl-1,3,4-oxadiazole-2-carboxamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: triethylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / N,N-dimethyl-formamide / 20 °C

2.1: trifluoroacetic acid / dichloromethane / 2 h / 20 °C

3.1: triethylamine / dichloromethane / 5 h / 20 °C / Cooling with ice

3.2: 20 °C / Cooling with ice

4.1: tetrahydrofuran / 2 h / 20 °C

5.1: potassium carbonate / 1-methyl-pyrrolidin-2-one / 4 h / 20 - 110 °C / Inert atmosphere

With potassium carbonate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; trifluoroacetic acid; In tetrahydrofuran; 1-methyl-pyrrolidin-2-one; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 1310807-72-7
tert-butyl 2-[(5-fluoropyridin-2-yl)carbonyl]hydrazinecarboxylate

: 1310805-86-7
5-[5-(3-{[(2S)-1-methoxypropan-2-yl]oxy}-5-[(1-methyl-1H-pyrazol-3-yl)carbamoyl]phenoxy)pyridin-2-yl]-N-methyl-1,3,4-oxadiazole-2-carboxamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: trifluoroacetic acid / dichloromethane / 2 h / 20 °C

2.1: triethylamine / dichloromethane / 5 h / 20 °C / Cooling with ice

2.2: 20 °C / Cooling with ice

3.1: tetrahydrofuran / 2 h / 20 °C

4.1: potassium carbonate / 1-methyl-pyrrolidin-2-one / 4 h / 20 - 110 °C / Inert atmosphere

With potassium carbonate; triethylamine; trifluoroacetic acid; In tetrahydrofuran; 1-methyl-pyrrolidin-2-one; dichloromethane;