(+/-)-tert-butyl 1-(1-(3-fluorobenzyl)-4-methyl-1H-imidazol-2-yl)-2-(7-methyl-2-((2-(trimethylsilyl)ethoxy)methyl)-2H-indazol-5-yl)ethylcarbamate

Base Information

Chemical Name:(+/-)-tert-butyl 1-(1-(3-fluorobenzyl)-4-methyl-1H-imidazol-2-yl)-2-(7-methyl-2-((2-(trimethylsilyl)ethoxy)methyl)-2H-indazol-5-yl)ethylcarbamate
CAS No.:855778-56-2
Molecular Formula:C₃₂H₄₄FN₅O₃Si
Molecular Weight:593.817
Hs Code.:

Synonyms:(+/-)-tert-butyl 1-(1-(3-fluorobenzyl)-4-methyl-1H-imidazol-2-yl)-2-(7-methyl-2-((2-(trimethylsilyl)ethoxy)methyl)-2H-indazol-5-yl)ethylcarbamate

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Chemical Property of (+/-)-tert-butyl 1-(1-(3-fluorobenzyl)-4-methyl-1H-imidazol-2-yl)-2-(7-methyl-2-((2-(trimethylsilyl)ethoxy)methyl)-2H-indazol-5-yl)ethylcarbamate

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Technology Process of (+/-)-tert-butyl 1-(1-(3-fluorobenzyl)-4-methyl-1H-imidazol-2-yl)-2-(7-methyl-2-((2-(trimethylsilyl)ethoxy)methyl)-2H-indazol-5-yl)ethylcarbamate

There total 5 articles about (+/-)-tert-butyl 1-(1-(3-fluorobenzyl)-4-methyl-1H-imidazol-2-yl)-2-(7-methyl-2-((2-(trimethylsilyl)ethoxy)methyl)-2H-indazol-5-yl)ethylcarbamate 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: 74.0%

: 855778-55-1
(+/-)-tert-butyl 1-(4-methyl-1H-imidazol-2-yl)-2-(7-methyl-2-((2-(trimethylsilyl)ethoxy)methyl)-2H-indazol-5-yl)ethylcarbamate

: 456-41-7
1-(Bromomethyl)-3-fluorobenzene

: 855778-56-2
(+/-)-tert-butyl 1-(1-(3-fluorobenzyl)-4-methyl-1H-imidazol-2-yl)-2-(7-methyl-2-((2-(trimethylsilyl)ethoxy)methyl)-2H-indazol-5-yl)ethylcarbamate

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2013.08.031

Reference yield:

: 121056-95-9,89524-98-1
trimethyl 2-(tert-butoxycarbonylamino)phosphonoacetate

: 855778-56-2
(+/-)-tert-butyl 1-(1-(3-fluorobenzyl)-4-methyl-1H-imidazol-2-yl)-2-(7-methyl-2-((2-(trimethylsilyl)ethoxy)methyl)-2H-indazol-5-yl)ethylcarbamate

Guidance literature:: Multi-step reaction with 5 steps

1: N,N,N',N'-tetramethylguanidine / tetrahydrofuran

2: palladium on activated charcoal; hydrogen / methanol

3: lithium borohydride / tetrahydrofuran

4: ammonium hydroxide / 1,4-dioxane; water / 80 °C

5: potassium carbonate / N,N-dimethyl-formamide

With ammonium hydroxide; lithium borohydride; palladium on activated charcoal; hydrogen; potassium carbonate; N,N,N',N'-tetramethylguanidine; In tetrahydrofuran; 1,4-dioxane; methanol; water; N,N-dimethyl-formamide; 1: |Horner-Wadsworth-Emmons Olefination;
DOI:10.1016/j.bmcl.2013.08.031

Reference yield:

: 855776-96-4
7-methyl-2-((2-(trimethylsilyl)ethoxy)methyl)-2H-indazole-5-carboxaldehyde

: 855778-56-2
(+/-)-tert-butyl 1-(1-(3-fluorobenzyl)-4-methyl-1H-imidazol-2-yl)-2-(7-methyl-2-((2-(trimethylsilyl)ethoxy)methyl)-2H-indazol-5-yl)ethylcarbamate

Guidance literature:: Multi-step reaction with 5 steps

1: N,N,N',N'-tetramethylguanidine / tetrahydrofuran

2: palladium on activated charcoal; hydrogen / methanol

3: lithium borohydride / tetrahydrofuran

4: ammonium hydroxide / 1,4-dioxane; water / 80 °C

5: potassium carbonate / N,N-dimethyl-formamide

With ammonium hydroxide; lithium borohydride; palladium on activated charcoal; hydrogen; potassium carbonate; N,N,N',N'-tetramethylguanidine; In tetrahydrofuran; 1,4-dioxane; methanol; water; N,N-dimethyl-formamide; 1: |Horner-Wadsworth-Emmons Olefination;
DOI:10.1016/j.bmcl.2013.08.031