1-[(R)-1-(tert-butyldimethylsilyloxy)-4-[6-(3-(4-chlorophenyl)propoxy)indol-1-yl]-2-butyl]imidazole-4-carboxamide

Base Information

Chemical Name:1-[(R)-1-(tert-butyldimethylsilyloxy)-4-[6-(3-(4-chlorophenyl)propoxy)indol-1-yl]-2-butyl]imidazole-4-carboxamide
CAS No.:294863-03-9
Molecular Formula:C₃₁H₄₁ClN₄O₃Si
Molecular Weight:581.23
Hs Code.:

Synonyms:1-[(R)-1-(tert-butyldimethylsilyloxy)-4-[6-(3-(4-chlorophenyl)propoxy)indol-1-yl]-2-butyl]imidazole-4-carboxamide

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Chemical Property of 1-[(R)-1-(tert-butyldimethylsilyloxy)-4-[6-(3-(4-chlorophenyl)propoxy)indol-1-yl]-2-butyl]imidazole-4-carboxamide

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Technology Process of 1-[(R)-1-(tert-butyldimethylsilyloxy)-4-[6-(3-(4-chlorophenyl)propoxy)indol-1-yl]-2-butyl]imidazole-4-carboxamide

There total 8 articles about 1-[(R)-1-(tert-butyldimethylsilyloxy)-4-[6-(3-(4-chlorophenyl)propoxy)indol-1-yl]-2-butyl]imidazole-4-carboxamide 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:

: 61440-60-6
methanesulfonic acid 3-(4-chlorophenyl)-propyl ester

: 294862-93-4
1-[(R)-1-(tert-butyldimethylsilyloxy)-4-(6-hydroxyindol-1-yl)-2-butyl]imidazole-4-carboxamide

: 294863-03-9
1-[(R)-1-(tert-butyldimethylsilyloxy)-4-[6-(3-(4-chlorophenyl)propoxy)indol-1-yl]-2-butyl]imidazole-4-carboxamide

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 80 - 90 ℃; for 24h;
DOI:10.1021/jm0306374

Reference yield:

: 6282-88-8
3-(p-chlorophenyl)propanol

: 294863-03-9
1-[(R)-1-(tert-butyldimethylsilyloxy)-4-[6-(3-(4-chlorophenyl)propoxy)indol-1-yl]-2-butyl]imidazole-4-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1: Et₃N / CH₂Cl₂ / 1 h / 0 °C

2: 90.5 mg / K₂CO₃ / dimethylformamide / 24 h / 80 - 90 °C

With potassium carbonate; triethylamine; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm0306374

Reference yield:

: (S)-4-(6-Benzyloxy-indol-1-yl)-butane-1,2-diol

: 294863-03-9
1-[(R)-1-(tert-butyldimethylsilyloxy)-4-[6-(3-(4-chlorophenyl)propoxy)indol-1-yl]-2-butyl]imidazole-4-carboxamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: 2.12 g / imidazole / dimethylformamide / 0 - 20 °C

2.1: Et₃N / CH₂Cl₂ / 1 h / 0 °C

3.1: NaH / dimethylformamide / 1 h / 70 °C

3.2: 982 mg / dimethylformamide / 24 h / 70 °C

4.1: 95.8 percent / cyclohexene; Pd(OH)2/C / ethanol / 1 h / Heating

5.1: 90.5 mg / K₂CO₃ / dimethylformamide / 24 h / 80 - 90 °C

With 1H-imidazole; palladium dihydroxide; sodium hydride; potassium carbonate; triethylamine; cyclohexene; In ethanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm0306374