2-[2,6-dimethyl-4-({[(5-methyl-2-phenyl-1,3-oxazol-4-yl) methyl][(5-methyl-1,3,4-thiadiazol-2-yl)methyl]amino}-methyl)phenoxy]-2-methylpropanoic acid

Base Information

Chemical Name:2-[2,6-dimethyl-4-({[(5-methyl-2-phenyl-1,3-oxazol-4-yl) methyl][(5-methyl-1,3,4-thiadiazol-2-yl)methyl]amino}-methyl)phenoxy]-2-methylpropanoic acid
CAS No.:1593269-90-9
Molecular Formula:C₂₈H₃₂N₄O₄S
Molecular Weight:520.652
Hs Code.:

Synonyms:2-[2,6-dimethyl-4-({[(5-methyl-2-phenyl-1,3-oxazol-4-yl) methyl][(5-methyl-1,3,4-thiadiazol-2-yl)methyl]amino}-methyl)phenoxy]-2-methylpropanoic acid

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Chemical Property of 2-[2,6-dimethyl-4-({[(5-methyl-2-phenyl-1,3-oxazol-4-yl) methyl][(5-methyl-1,3,4-thiadiazol-2-yl)methyl]amino}-methyl)phenoxy]-2-methylpropanoic acid

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Technology Process of 2-[2,6-dimethyl-4-({[(5-methyl-2-phenyl-1,3-oxazol-4-yl) methyl][(5-methyl-1,3,4-thiadiazol-2-yl)methyl]amino}-methyl)phenoxy]-2-methylpropanoic acid

There total 7 articles about 2-[2,6-dimethyl-4-({[(5-methyl-2-phenyl-1,3-oxazol-4-yl) methyl][(5-methyl-1,3,4-thiadiazol-2-yl)methyl]amino}-methyl)phenoxy]-2-methylpropanoic acid 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: 56.0%

: 1593269-94-3
ethyl 2-[2,6-dimethyl-4-({[(5-methyl-2-phenyl-1,3-oxazol-4-yl)-methyl][(5-methyl-1,3,4-thiadiazol-2-yl) methyl] amino}methyl)-phenoxy]-2-methylpropanoate

: 1593269-90-9
2-[2,6-dimethyl-4-({[(5-methyl-2-phenyl-1,3-oxazol-4-yl) methyl][(5-methyl-1,3,4-thiadiazol-2-yl)methyl]amino}-methyl)phenoxy]-2-methylpropanoic acid

Guidance literature:: With water; sodium hydroxide; In methanol; at 20 ℃;
DOI:10.1248/cpb.c13-00513

Reference yield:

: 639784-17-1
ethyl 2-(4-formyl-2,6-dimethylphenoxy)-2-methylpropanoate

: 1593269-90-9
2-[2,6-dimethyl-4-({[(5-methyl-2-phenyl-1,3-oxazol-4-yl) methyl][(5-methyl-1,3,4-thiadiazol-2-yl)methyl]amino}-methyl)phenoxy]-2-methylpropanoic acid

Guidance literature:: Multi-step reaction with 7 steps

1: magnesium sulfate / tetrahydrofuran / 4 h / Reflux

2: sodium tetrahydroborate / methanol / 4 h / 0 - 20 °C

3: potassium carbonate / acetonitrile / 24 h / Reflux

4: hydrogenchloride / dichloromethane; 1,4-dioxane / 14 h / 20 °C

5: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / N,N-dimethyl-formamide / 20 h / 20 °C

6: Lawessons reagent / tetrahydrofuran / 0.5 h / Reflux

7: sodium hydroxide; water / methanol / 20 °C

With Lawessons reagent; hydrogenchloride; sodium tetrahydroborate; water; magnesium sulfate; potassium carbonate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; sodium hydroxide; In tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1248/cpb.c13-00513

Reference yield:

: C₂₁H₃₁NO₅

: 1593269-90-9
2-[2,6-dimethyl-4-({[(5-methyl-2-phenyl-1,3-oxazol-4-yl) methyl][(5-methyl-1,3,4-thiadiazol-2-yl)methyl]amino}-methyl)phenoxy]-2-methylpropanoic acid

Guidance literature:: Multi-step reaction with 6 steps

1: sodium tetrahydroborate / methanol / 4 h / 0 - 20 °C

2: potassium carbonate / acetonitrile / 24 h / Reflux

3: hydrogenchloride / dichloromethane; 1,4-dioxane / 14 h / 20 °C

4: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / N,N-dimethyl-formamide / 20 h / 20 °C

5: Lawessons reagent / tetrahydrofuran / 0.5 h / Reflux

6: sodium hydroxide; water / methanol / 20 °C

With Lawessons reagent; hydrogenchloride; sodium tetrahydroborate; water; potassium carbonate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; sodium hydroxide; In tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1248/cpb.c13-00513