2-Pyrimidinamine, 4-[(5S)-5-[[[(1,1-dimethylethyl)diphenylsilyl]oxy]methyl]-2-(4-fluorophenyl) -6,7-dihydro-5H-pyrrolo[1,2-a]imidazol-3-yl]-N-propyl-

Base Information

Chemical Name:2-Pyrimidinamine, 4-[(5S)-5-[[[(1,1-dimethylethyl)diphenylsilyl]oxy]methyl]-2-(4-fluorophenyl) -6,7-dihydro-5H-pyrrolo[1,2-a]imidazol-3-yl]-N-propyl-
CAS No.:926660-11-9
Molecular Formula:C36H40FN5OSi
Molecular Weight:605.83
Hs Code.:

2-Pyrimidinamine,
4-[(5S)-5-[[[(1,1-dimethylethyl)diphenylsilyl]oxy]methyl]-2-(4-fluorophenyl)
-6,7-dihydro-5H-pyrrolo[1,2-a]imidazol-3-yl]-N-propyl-

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Chemical Property of 2-Pyrimidinamine, 4-[(5S)-5-[[[(1,1-dimethylethyl)diphenylsilyl]oxy]methyl]-2-(4-fluorophenyl) -6,7-dihydro-5H-pyrrolo[1,2-a]imidazol-3-yl]-N-propyl-

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Technology Process of 2-Pyrimidinamine, 4-[(5S)-5-[[[(1,1-dimethylethyl)diphenylsilyl]oxy]methyl]-2-(4-fluorophenyl) -6,7-dihydro-5H-pyrrolo[1,2-a]imidazol-3-yl]-N-propyl-

There total 4 articles about 2-Pyrimidinamine, 4-[(5S)-5-[[[(1,1-dimethylethyl)diphenylsilyl]oxy]methyl]-2-(4-fluorophenyl) -6,7-dihydro-5H-pyrrolo[1,2-a]imidazol-3-yl]-N-propyl- 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: 78.0%

: 926660-10-8
5-(tert-butyl-diphenyl-silanyloxymethyl)-2-(4-fluoro-phenyl)-3-(2-methanesulfonyl-pyrimidin-4-yl)-6,7-dihydro-5H-pyrrolo[1,2-a]imidazole

: 107-10-8,42939-71-9
propylamine

: 926660-11-9
{4-[5-(tert-butyl-diphenyl-silanyloxymethyl)-2-(4-fluoro-phenyl)-6,7-dihydro-5H-pyrrolo[1,2-a]imidazol-3-yl]-pyrimidin-2-yl}-propyl-amine

Guidance literature:: at 20 ℃; for 8h;
DOI:10.1021/ja0676004

Reference yield:

: 926659-97-4
(S)-5-((tert-butyldiphenylsilyloxy)methyl)-2-(4-fluorophenyl)-6,7-dihydro-5Hpyrrolo[1,2-a]imidazole

: 926660-11-9
{4-[5-(tert-butyl-diphenyl-silanyloxymethyl)-2-(4-fluoro-phenyl)-6,7-dihydro-5H-pyrrolo[1,2-a]imidazol-3-yl]-pyrimidin-2-yl}-propyl-amine

Guidance literature:: Multi-step reaction with 4 steps

1: Br₂ / CH₂Cl₂ / 0.25 h / -78 °C

2: 85 percent / triphenylphosphine; LiCl; CuI / Pd₂(dba)2*CHCl₃ / dioxane / 5.5 h / 170 °C

3: 79 percent / oxone / tetrahydrofuran; H₂O / 5 h / 20 °C

4: 78 percent / 8 h / 20 °C

With Oxone; copper(l) iodide; bromine; triphenylphosphine; lithium chloride; Pd₂(dibenzylideneacetone)2*CHCl₃; In tetrahydrofuran; 1,4-dioxane; dichloromethane; water;
DOI:10.1021/ja0676004

Reference yield:

: 926660-08-4
(S)-2-[4-(4-fluorophenyl)-imidazolyl]-but-3-enol

: 926660-11-9
{4-[5-(tert-butyl-diphenyl-silanyloxymethyl)-2-(4-fluoro-phenyl)-6,7-dihydro-5H-pyrrolo[1,2-a]imidazol-3-yl]-pyrimidin-2-yl}-propyl-amine

Guidance literature:: Multi-step reaction with 6 steps

1: 98 percent / iPr₂NEt; 4-dimethylaminopyridine / CH₂Cl₂ / 8 h / 20 °C

2: tricyclohexylphosphine; MgBr₂ / [RhCl(coe)2]2 / toluene / 5.5 h / 180 °C

3: Br₂ / CH₂Cl₂ / 0.25 h / -78 °C

4: 85 percent / triphenylphosphine; LiCl; CuI / Pd₂(dba)2*CHCl₃ / dioxane / 5.5 h / 170 °C

5: 79 percent / oxone / tetrahydrofuran; H₂O / 5 h / 20 °C

6: 78 percent / 8 h / 20 °C

With dmap; Oxone; copper(l) iodide; bromine; N-ethyl-N,N-diisopropylamine; triphenylphosphine; lithium chloride; magnesium bromide; tricyclohexylphosphine; Pd₂(dibenzylideneacetone)2*CHCl₃; [RhCl(coe)2]2; In tetrahydrofuran; 1,4-dioxane; dichloromethane; water; toluene;
DOI:10.1021/ja0676004