3-hydroxy-5-{(1S)-2-methoxy-(1-methylethyl)oxy}-N-(3-methyl-1,2,4-thiadiazol-2-yl)benzamide

Base Information

Chemical Name:3-hydroxy-5-{(1S)-2-methoxy-(1-methylethyl)oxy}-N-(3-methyl-1,2,4-thiadiazol-2-yl)benzamide
CAS No.:863504-89-6
Molecular Formula:C₁₄H₁₇N₃O₄S
Molecular Weight:323.373
Hs Code.:

Synonyms:3-hydroxy-5-{(1S)-2-methoxy-(1-methylethyl)oxy}-N-(3-methyl-1,2,4-thiadiazol-2-yl)benzamide

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Chemical Property of 3-hydroxy-5-{(1S)-2-methoxy-(1-methylethyl)oxy}-N-(3-methyl-1,2,4-thiadiazol-2-yl)benzamide

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Technology Process of 3-hydroxy-5-{(1S)-2-methoxy-(1-methylethyl)oxy}-N-(3-methyl-1,2,4-thiadiazol-2-yl)benzamide

There total 6 articles about 3-hydroxy-5-{(1S)-2-methoxy-(1-methylethyl)oxy}-N-(3-methyl-1,2,4-thiadiazol-2-yl)benzamide 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:

: 863504-90-9
3-{(1S)-2-methoxy-(1-methylethyl)oxy}-5-{phenylmethyloxy}-N-(3-methyl-1,2,4-thiadiazol-2-yl)benzamide

: 863504-89-6
3-hydroxy-5-{(1S)-2-methoxy-(1-methylethyl)oxy}-N-(3-methyl-1,2,4-thiadiazol-2-yl)benzamide

Guidance literature:: With methyl-phenyl-thioether; trifluoroacetic acid; at 20 ℃; for 16h;

Reference yield:

: 2150-44-9
1-carbomethoxy-3,5-dihydroxybenzene

: 863504-89-6
3-hydroxy-5-{(1S)-2-methoxy-(1-methylethyl)oxy}-N-(3-methyl-1,2,4-thiadiazol-2-yl)benzamide

Guidance literature:: Multi-step reaction with 6 steps

1.1: potassium carbonate / N,N-dimethyl-formamide / 20 °C

2.1: polymer supported triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 0.5 h / 0 °C

3.1: sodium hydroxide / tetrahydrofuran; methanol; water / 4 h / 20 °C

3.2: pH 4

4.1: oxalyl dichloride / dichloromethane / 4 h / 20 °C

5.1: triethylamine / dichloromethane / 16 h / 0 - 20 °C

6.1: methyl-phenyl-thioether; trifluoroacetic acid / 16 h / 20 °C

With sodium hydroxide; oxalyl dichloride; polymer supported triphenylphosphine; methyl-phenyl-thioether; di-isopropyl azodicarboxylate; potassium carbonate; triethylamine; trifluoroacetic acid; In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide;

Reference yield:

: 54915-31-0
methyl 3-(benzyloxy)-5-hydroxybenzoate

: 863504-89-6
3-hydroxy-5-{(1S)-2-methoxy-(1-methylethyl)oxy}-N-(3-methyl-1,2,4-thiadiazol-2-yl)benzamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: polymer supported triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 0.5 h / 0 °C

2.1: sodium hydroxide / tetrahydrofuran; methanol; water / 4 h / 20 °C

2.2: pH 4

3.1: oxalyl dichloride / dichloromethane / 4 h / 20 °C

4.1: triethylamine / dichloromethane / 16 h / 0 - 20 °C

5.1: methyl-phenyl-thioether; trifluoroacetic acid / 16 h / 20 °C

With sodium hydroxide; oxalyl dichloride; polymer supported triphenylphosphine; methyl-phenyl-thioether; di-isopropyl azodicarboxylate; triethylamine; trifluoroacetic acid; In tetrahydrofuran; methanol; dichloromethane; water;