1-(4-methoxy-benzyl)-3-(4-methoxy-phenyl)-5-(2-trimethylsilanyl-ethoxy)-1H-pyrrolo[3,2-b]pyridine

Base Information

Chemical Name:1-(4-methoxy-benzyl)-3-(4-methoxy-phenyl)-5-(2-trimethylsilanyl-ethoxy)-1H-pyrrolo[3,2-b]pyridine
CAS No.:361456-07-7
Molecular Formula:C₂₇H₃₂N₂O₃Si
Molecular Weight:460.648
Hs Code.:

1-(4-methoxy-benzyl)-3-(4-methoxy-phenyl)-5-(2-trimethylsilanyl-ethoxy)-1<i>H</i>-pyrrolo[3,2-<i>b</i>]pyridine

Synonyms:1-(4-methoxy-benzyl)-3-(4-methoxy-phenyl)-5-(2-trimethylsilanyl-ethoxy)-1H-pyrrolo[3,2-b]pyridine

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Chemical Property of 1-(4-methoxy-benzyl)-3-(4-methoxy-phenyl)-5-(2-trimethylsilanyl-ethoxy)-1H-pyrrolo[3,2-b]pyridine

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Technology Process of 1-(4-methoxy-benzyl)-3-(4-methoxy-phenyl)-5-(2-trimethylsilanyl-ethoxy)-1H-pyrrolo[3,2-b]pyridine

There total 8 articles about 1-(4-methoxy-benzyl)-3-(4-methoxy-phenyl)-5-(2-trimethylsilanyl-ethoxy)-1H-pyrrolo[3,2-b]pyridine 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: 31.0%

: 2746-25-0
p-Methoxybenzyl bromide

: 361456-04-4
3-(4-methoxy-phenyl)-5-(2-trimethylsilanyl-ethoxy)-1H-pyrrolo[3,2-b]pyridine

: 361456-07-7
1-(4-methoxy-benzyl)-3-(4-methoxy-phenyl)-5-(2-trimethylsilanyl-ethoxy)-1H-pyrrolo[3,2-b]pyridine

Guidance literature:: With sodium hydride; In tetrahydrofuran; at 20 ℃; for 18h;
DOI:10.1016/S0960-894X(01)00022-1

Reference yield:

: 4548-45-2
2-chloro-5-nitropyridine

: 361456-07-7
1-(4-methoxy-benzyl)-3-(4-methoxy-phenyl)-5-(2-trimethylsilanyl-ethoxy)-1H-pyrrolo[3,2-b]pyridine

Guidance literature:: Multi-step reaction with 6 steps

1: 65 percent / t-BuOK / dimethylformamide / 20 °C

2: 87 percent / t-BuOK / tetrahydrofuran / 3 h / -10 °C

3: 76 percent / H₂ / Pd/C / ethanol

4: 100 percent / NIS / tetrahydrofuran / 2 h / 20 °C

5: 71 percent / PdCl₂(dppf); 2 N aq. Na₂CO₃ / ethanol / 3 h / Heating

6: 31 percent / NaH / tetrahydrofuran / 18 h / 20 °C

With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; N-iodo-succinimide; potassium tert-butylate; hydrogen; sodium hydride; sodium carbonate; palladium on activated charcoal; In tetrahydrofuran; ethanol; N,N-dimethyl-formamide; 5: Suzuki cross-coupling reaction;
DOI:10.1016/S0960-894X(01)00022-1

Reference yield:

: 2916-68-9
2-(Trimethylsilyl)ethanol

: 361456-07-7
1-(4-methoxy-benzyl)-3-(4-methoxy-phenyl)-5-(2-trimethylsilanyl-ethoxy)-1H-pyrrolo[3,2-b]pyridine

Guidance literature:: Multi-step reaction with 6 steps

1: 65 percent / t-BuOK / dimethylformamide / 20 °C

2: 87 percent / t-BuOK / tetrahydrofuran / 3 h / -10 °C

3: 76 percent / H₂ / Pd/C / ethanol

4: 100 percent / NIS / tetrahydrofuran / 2 h / 20 °C

5: 71 percent / PdCl₂(dppf); 2 N aq. Na₂CO₃ / ethanol / 3 h / Heating

6: 31 percent / NaH / tetrahydrofuran / 18 h / 20 °C

With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; N-iodo-succinimide; potassium tert-butylate; hydrogen; sodium hydride; sodium carbonate; palladium on activated charcoal; In tetrahydrofuran; ethanol; N,N-dimethyl-formamide; 5: Suzuki cross-coupling reaction;
DOI:10.1016/S0960-894X(01)00022-1