1-(4-amino-2-fluorophenyl)-4-(tert-butyldimethylsilanyloxymethyl)-1H-imidazole

Base Information

Chemical Name:1-(4-amino-2-fluorophenyl)-4-(tert-butyldimethylsilanyloxymethyl)-1H-imidazole
CAS No.:196299-02-2
Molecular Formula:C₁₆H₂₄FN₃OSi
Molecular Weight:321.47
Hs Code.:

Synonyms:1-(4-amino-2-fluorophenyl)-4-(tert-butyldimethylsilanyloxymethyl)-1H-imidazole

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 1-(4-amino-2-fluorophenyl)-4-(tert-butyldimethylsilanyloxymethyl)-1H-imidazole

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Technology Process of 1-(4-amino-2-fluorophenyl)-4-(tert-butyldimethylsilanyloxymethyl)-1H-imidazole

There total 5 articles about 1-(4-amino-2-fluorophenyl)-4-(tert-butyldimethylsilanyloxymethyl)-1H-imidazole 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: 80.0%

: 196299-00-0
4-({[tert-butyldimethylsilyl]oxy}methyl)-1-(2-fluoro-4-nitrophenyl)-1H-imidazole

: 196299-02-2
1-(4-amino-2-fluorophenyl)-4-(tert-butyldimethylsilanyloxymethyl)-1H-imidazole

Guidance literature:: With sodium tetrahydroborate; nickel dichloride; In methanol; at 20 ℃; for 1h;

Reference yield:

: 369-34-6
3,4-difluoronitrobenzene

: 196299-02-2
1-(4-amino-2-fluorophenyl)-4-(tert-butyldimethylsilanyloxymethyl)-1H-imidazole

Guidance literature:: Multi-step reaction with 3 steps

1: 47 percent / K₂CO₃ / acetone / 24 h / Heating

2: 64 percent / imidazole / dimethylformamide / 0 - 20 °C

3: H₂ / tetrahydrofuran / 18 h

With 1H-imidazole; hydrogen; potassium carbonate; In tetrahydrofuran; N,N-dimethyl-formamide; acetone; 1: Substitution / 2: silylation / 3: Reduction;
DOI:10.1021/jm990373e

Reference yield:

: 196298-99-4
[1-(2-fluoro-4-nitrophenyl)-1H-imidazol-4-yl]methanol

: 196299-02-2
1-(4-amino-2-fluorophenyl)-4-(tert-butyldimethylsilanyloxymethyl)-1H-imidazole

Guidance literature:: Multi-step reaction with 2 steps

1: 64 percent / imidazole / dimethylformamide / 0 - 20 °C

2: H₂ / tetrahydrofuran / 18 h

With 1H-imidazole; hydrogen; In tetrahydrofuran; N,N-dimethyl-formamide; 1: silylation / 2: Reduction;
DOI:10.1021/jm990373e