3-[2-{3-(tert-butyldimethylsilyloxy)cyclohexyl}-3-oxo-2,3-dihydropyridazin-6-yl]-2-phenylpyrazolo[1,5-a]-pyridine

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Chemical Name:3-[2-{3-(tert-butyldimethylsilyloxy)cyclohexyl}-3-oxo-2,3-dihydropyridazin-6-yl]-2-phenylpyrazolo[1,5-a]-pyridine
CAS No.:171050-75-2
Molecular Formula:C₂₉H₃₆N₄O₂Si
Molecular Weight:500.716
Hs Code.:

Synonyms:3-[2-{3-(tert-butyldimethylsilyloxy)cyclohexyl}-3-oxo-2,3-dihydropyridazin-6-yl]-2-phenylpyrazolo[1,5-a]-pyridine

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Chemical Property of 3-[2-{3-(tert-butyldimethylsilyloxy)cyclohexyl}-3-oxo-2,3-dihydropyridazin-6-yl]-2-phenylpyrazolo[1,5-a]-pyridine

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Technology Process of 3-[2-{3-(tert-butyldimethylsilyloxy)cyclohexyl}-3-oxo-2,3-dihydropyridazin-6-yl]-2-phenylpyrazolo[1,5-a]-pyridine

There total 5 articles about 3-[2-{3-(tert-butyldimethylsilyloxy)cyclohexyl}-3-oxo-2,3-dihydropyridazin-6-yl]-2-phenylpyrazolo[1,5-a]-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:

: tert-butyl((3-iodocyclohexyl)oxy)dimethylsilane

: 131185-06-3
3-(3-oxo-2,3-dihydropyridazin-6-yl)-2-phenylpyrazolo<1,5-a>pyridine

: 171050-75-2
3-[2-{3-(tert-butyldimethylsilyloxy)cyclohexyl}-3-oxo-2,3-dihydropyridazin-6-yl]-2-phenylpyrazolo[1,5-a]-pyridine

Guidance literature:: With 18-crown-6 ether; potassium tert-butylate; In ethoxycarbonylmethylene; dichloromethane; water; N,N-dimethyl-formamide; at 20 ℃; for 2h;

Reference yield:

: 1028748-71-1
3-((tert-butyldimethylsilyl)oxy)cyclohexan-1-ol

: 171050-75-2
3-[2-{3-(tert-butyldimethylsilyloxy)cyclohexyl}-3-oxo-2,3-dihydropyridazin-6-yl]-2-phenylpyrazolo[1,5-a]-pyridine

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine / dichloromethane

2: sodium iodide / N,N-dimethyl-formamide / 3 h / 100 °C

3: 18-crown-6 ether; potassium tert-butylate / ethoxycarbonylmethylene; dichloromethane; water; N,N-dimethyl-formamide / 2 h / 20 °C

With 18-crown-6 ether; potassium tert-butylate; triethylamine; sodium iodide; In ethoxycarbonylmethylene; dichloromethane; water; N,N-dimethyl-formamide;

Reference yield:

: 504-01-8
cyclohexane-1,3-diol

: 171050-75-2
3-[2-{3-(tert-butyldimethylsilyloxy)cyclohexyl}-3-oxo-2,3-dihydropyridazin-6-yl]-2-phenylpyrazolo[1,5-a]-pyridine

Guidance literature:: Multi-step reaction with 4 steps

1: 1H-imidazole / tetrahydrofuran; dichloromethane / 20 °C

2: triethylamine / dichloromethane

3: sodium iodide / N,N-dimethyl-formamide / 3 h / 100 °C

4: 18-crown-6 ether; potassium tert-butylate / ethoxycarbonylmethylene; dichloromethane; water; N,N-dimethyl-formamide / 2 h / 20 °C

With 1H-imidazole; 18-crown-6 ether; potassium tert-butylate; triethylamine; sodium iodide; In tetrahydrofuran; ethoxycarbonylmethylene; dichloromethane; water; N,N-dimethyl-formamide;