4-[4-(4-fluorophenyl)-1-{1-[(1R)-1-isoxazol-3-ylethyl]piperidin-4-yl}-1H-imidazol-5-yl]pyrimidine

Base Information

Chemical Name:4-[4-(4-fluorophenyl)-1-{1-[(1R)-1-isoxazol-3-ylethyl]piperidin-4-yl}-1H-imidazol-5-yl]pyrimidine
CAS No.:1293395-72-8
Molecular Formula:C₂₃H₂₃FN₆O
Molecular Weight:418.474
Hs Code.:

Synonyms:4-[4-(4-fluorophenyl)-1-{1-[(1R)-1-isoxazol-3-ylethyl]piperidin-4-yl}-1H-imidazol-5-yl]pyrimidine

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Chemical Property of 4-[4-(4-fluorophenyl)-1-{1-[(1R)-1-isoxazol-3-ylethyl]piperidin-4-yl}-1H-imidazol-5-yl]pyrimidine

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Technology Process of 4-[4-(4-fluorophenyl)-1-{1-[(1R)-1-isoxazol-3-ylethyl]piperidin-4-yl}-1H-imidazol-5-yl]pyrimidine

There total 6 articles about 4-[4-(4-fluorophenyl)-1-{1-[(1R)-1-isoxazol-3-ylethyl]piperidin-4-yl}-1H-imidazol-5-yl]pyrimidine 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: 4.0%

: 1293396-28-7
1-isoxazol-3-ylethyl methanesulfonate

: 1293396-31-2
4-[4-(4-Fluorophenyl)-1-piperidin-4-yl-1H-imidazol-5-yl]pyrimidine

: 1293395-72-8
4-[4-(4-fluorophenyl)-1-{1-[(1R)-1-isoxazol-3-ylethyl]piperidin-4-yl}-1H-imidazol-5-yl]pyrimidine

: 1293395-73-9
4-[4-(4-fluorophenyl)-1-{1-[(1S)-1-isoxazol-3-ylethyl]piperidin-4-yl}-1H-imidazol-5-yl]pyrimidine

Guidance literature:: With caesium carbonate; In N,N-dimethyl-formamide; at 60 ℃; for 18h;

Reference yield:

: 25746-87-6
acetal dimethylique du pyrimidine-4 carboxaldehyde

: 1293395-72-8
4-[4-(4-fluorophenyl)-1-{1-[(1R)-1-isoxazol-3-ylethyl]piperidin-4-yl}-1H-imidazol-5-yl]pyrimidine

: 1293395-73-9
4-[4-(4-fluorophenyl)-1-{1-[(1S)-1-isoxazol-3-ylethyl]piperidin-4-yl}-1H-imidazol-5-yl]pyrimidine

Guidance literature:: Multi-step reaction with 5 steps

1.1: hydrogenchloride / water / 24 h / 60 - 70 °C

2.1: tert-butyl methyl ether / 2.5 h

3.1: potassium carbonate / N,N-dimethyl-formamide / 18 h

4.1: trifluoroacetic acid / dichloromethane / 18 h

4.2: pH 12

5.1: caesium carbonate / N,N-dimethyl-formamide / 18 h / 60 °C

With hydrogenchloride; potassium carbonate; caesium carbonate; trifluoroacetic acid; In dichloromethane; tert-butyl methyl ether; water; N,N-dimethyl-formamide;

Reference yield:

: 2435-50-9
pyrimidine-4-carboxaldehyde

: 1293395-72-8
4-[4-(4-fluorophenyl)-1-{1-[(1R)-1-isoxazol-3-ylethyl]piperidin-4-yl}-1H-imidazol-5-yl]pyrimidine

: 1293395-73-9
4-[4-(4-fluorophenyl)-1-{1-[(1S)-1-isoxazol-3-ylethyl]piperidin-4-yl}-1H-imidazol-5-yl]pyrimidine

Guidance literature:: Multi-step reaction with 4 steps

1.1: tert-butyl methyl ether / 2.5 h

2.1: potassium carbonate / N,N-dimethyl-formamide / 18 h

3.1: trifluoroacetic acid / dichloromethane / 18 h

3.2: pH 12

4.1: caesium carbonate / N,N-dimethyl-formamide / 18 h / 60 °C

With potassium carbonate; caesium carbonate; trifluoroacetic acid; In dichloromethane; tert-butyl methyl ether; N,N-dimethyl-formamide;