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methyl 3-(2-(4-methoxyphenyl)-3-(1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazol-2-yl)pyrazolo[1,5-a]pyridin-5-yl)-4-methylbenzoate

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  • Chemical Name:methyl 3-(2-(4-methoxyphenyl)-3-(1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazol-2-yl)pyrazolo[1,5-a]pyridin-5-yl)-4-methylbenzoate
  • CAS No.:1383854-50-9
  • Molecular Formula:C32H36N4O4Si
  • Molecular Weight:568.748
  • Hs Code.:
methyl 3-(2-(4-methoxyphenyl)-3-(1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazol-2-yl)pyrazolo[1,5-a]pyridin-5-yl)-4-methylbenzoate

Synonyms:methyl 3-(2-(4-methoxyphenyl)-3-(1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazol-2-yl)pyrazolo[1,5-a]pyridin-5-yl)-4-methylbenzoate

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Chemical Property of methyl 3-(2-(4-methoxyphenyl)-3-(1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazol-2-yl)pyrazolo[1,5-a]pyridin-5-yl)-4-methylbenzoate
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Technology Process of methyl 3-(2-(4-methoxyphenyl)-3-(1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazol-2-yl)pyrazolo[1,5-a]pyridin-5-yl)-4-methylbenzoate

There total 11 articles about methyl 3-(2-(4-methoxyphenyl)-3-(1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazol-2-yl)pyrazolo[1,5-a]pyridin-5-yl)-4-methylbenzoate 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:
Guidance literature:
Multi-step reaction with 8 steps
1.1: lithium hexamethyldisilazane / tetrahydrofuran / 18 h / 20 °C
2.1: hydroxylamine hydrochloride; sodium hydroxide / methanol; water / 2 h / Reflux
3.1: trifluoroacetic anhydride / 1,2-dimethoxyethane / 0.67 h / 20 °C / Inert atmosphere
3.2: 6.5 h / 0 °C / Inert atmosphere
3.3: 16 h / 70 °C / Inert atmosphere
4.1: potassium acetate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2 / 1,4-dioxane / 18 h / 100 °C / Inert atmosphere; sealed tube
5.1: cesium fluoride / dichlorobis(chlorodi-tert-butylphosphine) palladium(II) / N,N-dimethyl-formamide / 18 h / 90 °C
6.1: N-iodo-succinimide / dichloromethane; acetonitrile / 2 h / 20 °C
7.1: XPhos / dichloro bis(acetonitrile) palladium(II) / 1,4-dioxane / 2 h / 110 °C / microwave tube; Inert atmosphere; sealed tube
8.1: potassium phosphate / tris-(dibenzylideneacetone)dipalladium(0) / tetrahydrofuran; water / 18 h / 90 °C / Inert atmosphere; microwave tube; sealed tube
With potassium phosphate; N-iodo-succinimide; hydroxylamine hydrochloride; potassium acetate; cesium fluoride; trifluoroacetic anhydride; sodium hydroxide; lithium hexamethyldisilazane; XPhos; dichloro bis(acetonitrile) palladium(II); tris-(dibenzylideneacetone)dipalladium(0); dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; dichlorobis(chlorodi-tert-butylphosphine) palladium(II); In tetrahydrofuran; 1,4-dioxane; methanol; 1,2-dimethoxyethane; dichloromethane; water; N,N-dimethyl-formamide; acetonitrile;
Guidance literature:
Multi-step reaction with 3 steps
1.1: sodium hydride / tetrahydrofuran; mineral oil / 0.75 h / 0 - 20 °C
1.2: 18 h / 20 °C
1.3: 20 °C
2.1: n-butyllithium / tetrahydrofuran; hexane / 0.75 h / -40 °C
2.2: 0.33 h / 20 °C
2.3: 20 °C
3.1: potassium phosphate / tris-(dibenzylideneacetone)dipalladium(0) / tetrahydrofuran; water / 18 h / 90 °C / Inert atmosphere; microwave tube; sealed tube
With potassium phosphate; n-butyllithium; sodium hydride; tris-(dibenzylideneacetone)dipalladium(0); In tetrahydrofuran; hexane; water; mineral oil;
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