methyl 2-tert-butoxy-2-(1-(2-((tert-butyldimethylsilyl)oxy)ethyl)-4-(4-chlorophenyl)-2,3,6-trimethyl-1H-pyrrolo[2,3-b]pyridin-5-yl)acetate

Base Information

Chemical Name:methyl 2-tert-butoxy-2-(1-(2-((tert-butyldimethylsilyl)oxy)ethyl)-4-(4-chlorophenyl)-2,3,6-trimethyl-1H-pyrrolo[2,3-b]pyridin-5-yl)acetate
CAS No.:1436855-92-3
Molecular Formula:C₃₁H₄₅ClN₂O₄Si
Molecular Weight:573.248
Hs Code.:

Synonyms:methyl 2-tert-butoxy-2-(1-(2-((tert-butyldimethylsilyl)oxy)ethyl)-4-(4-chlorophenyl)-2,3,6-trimethyl-1H-pyrrolo[2,3-b]pyridin-5-yl)acetate

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Chemical Property of methyl 2-tert-butoxy-2-(1-(2-((tert-butyldimethylsilyl)oxy)ethyl)-4-(4-chlorophenyl)-2,3,6-trimethyl-1H-pyrrolo[2,3-b]pyridin-5-yl)acetate

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Technology Process of methyl 2-tert-butoxy-2-(1-(2-((tert-butyldimethylsilyl)oxy)ethyl)-4-(4-chlorophenyl)-2,3,6-trimethyl-1H-pyrrolo[2,3-b]pyridin-5-yl)acetate

There total 15 articles about methyl 2-tert-butoxy-2-(1-(2-((tert-butyldimethylsilyl)oxy)ethyl)-4-(4-chlorophenyl)-2,3,6-trimethyl-1H-pyrrolo[2,3-b]pyridin-5-yl)acetate 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: 27.0%

: 1436855-56-9
methyl 2-tert-butoxy-2-(4-(4-chlorophenyl)-2,3,6-trimethyl-1H-pyrrolo[2,3-b]pyridin-5-yl)acetate

: 101166-65-8
2-tert-butyldimethylsilyloxyethyl iodide

: 1436855-92-3
methyl 2-tert-butoxy-2-(1-(2-((tert-butyldimethylsilyl)oxy)ethyl)-4-(4-chlorophenyl)-2,3,6-trimethyl-1H-pyrrolo[2,3-b]pyridin-5-yl)acetate

Guidance literature:: With tetrabutylammomium bromide; potassium hydroxide; In dichloromethane; at 30 ℃; for 4h;

Reference yield:

: 1436855-52-5
4-(4-chlorophenyl)-1-(4-methoxybenzyl)-2,3,6-trimethyl-1H-pyrrolo[2,3-b]pyridine-5-carboaldehyde

: 1436855-92-3
methyl 2-tert-butoxy-2-(1-(2-((tert-butyldimethylsilyl)oxy)ethyl)-4-(4-chlorophenyl)-2,3,6-trimethyl-1H-pyrrolo[2,3-b]pyridin-5-yl)acetate

Guidance literature:: Multi-step reaction with 5 steps

1: zinc(II) iodide / dichloromethane / 4 h / 0 - 25 °C / Inert atmosphere

2: hydrogenchloride / water / 18 h / 100 °C

3: sulfuric acid / 18 h / Reflux

4: perchloric acid / dichloromethane; ethyl acetate / 4 h / 0 - 20 °C

5: tetrabutylammomium bromide; potassium hydroxide / dichloromethane / 4 h / 30 °C

With hydrogenchloride; perchloric acid; sulfuric acid; tetrabutylammomium bromide; potassium hydroxide; zinc(II) iodide; In dichloromethane; water; ethyl acetate;

Reference yield:

: 1436855-51-4
(4-(4-chlorophenyl)-1-(4-methoxybenzyl)-2,3,6-trimethyl-1H-pyrrolo[2,3-b]pyridin-5-yl)methanol

: 1436855-92-3
methyl 2-tert-butoxy-2-(1-(2-((tert-butyldimethylsilyl)oxy)ethyl)-4-(4-chlorophenyl)-2,3,6-trimethyl-1H-pyrrolo[2,3-b]pyridin-5-yl)acetate

Guidance literature:: Multi-step reaction with 6 steps

1: sulfur trioxide pyridine complex; triethylamine / dimethyl sulfoxide / 3 h / 10 - 25 °C

2: zinc(II) iodide / dichloromethane / 4 h / 0 - 25 °C / Inert atmosphere

3: hydrogenchloride / water / 18 h / 100 °C

4: sulfuric acid / 18 h / Reflux

5: perchloric acid / dichloromethane; ethyl acetate / 4 h / 0 - 20 °C

6: tetrabutylammomium bromide; potassium hydroxide / dichloromethane / 4 h / 30 °C

With hydrogenchloride; perchloric acid; sulfuric acid; tetrabutylammomium bromide; sulfur trioxide pyridine complex; triethylamine; potassium hydroxide; zinc(II) iodide; In dichloromethane; water; dimethyl sulfoxide; ethyl acetate;