(R,R)-2-methyl-propane-2-sulfinic acid [2-[6-(3-chloro-4-trifluoromethyl-phenyl)pyrimidin-4-ylamino]-1-(4-fluoro-phenyl)-ethyl]-amide

Base Information

Chemical Name:(R,R)-2-methyl-propane-2-sulfinic acid [2-[6-(3-chloro-4-trifluoromethyl-phenyl)pyrimidin-4-ylamino]-1-(4-fluoro-phenyl)-ethyl]-amide
CAS No.:1267688-22-1
Molecular Formula:C₂₃H₂₃ClF₄N₄OS
Molecular Weight:514.974
Hs Code.:

Synonyms:(R,R)-2-methyl-propane-2-sulfinic acid [2-[6-(3-chloro-4-trifluoromethyl-phenyl)pyrimidin-4-ylamino]-1-(4-fluoro-phenyl)-ethyl]-amide

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Chemical Property of (R,R)-2-methyl-propane-2-sulfinic acid [2-[6-(3-chloro-4-trifluoromethyl-phenyl)pyrimidin-4-ylamino]-1-(4-fluoro-phenyl)-ethyl]-amide

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Technology Process of (R,R)-2-methyl-propane-2-sulfinic acid [2-[6-(3-chloro-4-trifluoromethyl-phenyl)pyrimidin-4-ylamino]-1-(4-fluoro-phenyl)-ethyl]-amide

There total 5 articles about (R,R)-2-methyl-propane-2-sulfinic acid [2-[6-(3-chloro-4-trifluoromethyl-phenyl)pyrimidin-4-ylamino]-1-(4-fluoro-phenyl)-ethyl]-amide 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: 50.0%

: 1267688-21-0
(R,R)-2-methyl-propane-2-sulfinic acid [2-amino-1-(4-fluoro-phenyl)-ethyl]-amide

: 954223-40-6
4-chloro-6-(3-chloro-4-trifluoromethylphenyl)-pyrimidine

: 1267688-22-1
(R,R)-2-methyl-propane-2-sulfinic acid [2-[6-(3-chloro-4-trifluoromethyl-phenyl)pyrimidin-4-ylamino]-1-(4-fluoro-phenyl)-ethyl]-amide

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 80 ℃; for 16h; Inert atmosphere;

Reference yield:

: 459-57-4
4-fluorobenzaldehyde

: 1267688-22-1
(R,R)-2-methyl-propane-2-sulfinic acid [2-[6-(3-chloro-4-trifluoromethyl-phenyl)pyrimidin-4-ylamino]-1-(4-fluoro-phenyl)-ethyl]-amide

Guidance literature:: Multi-step reaction with 4 steps

1.1: titanium(IV) tetraethanolate / tetrahydrofuran / 16 h / 20 °C / Inert atmosphere

2.1: potassium tert-butylate / tetrahydrofuran / 0 °C / Inert atmosphere

2.2: 16 h / 0 - 20 °C / Inert atmosphere

2.3: 20 °C / pH 5 / Inert atmosphere

3.1: zinc; water; ammonium chloride / acetone / 0.17 h / 20 °C / Inert atmosphere

4.1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 16 h / 80 °C / Inert atmosphere

With potassium tert-butylate; water; ammonium chloride; N-ethyl-N,N-diisopropylamine; zinc; titanium(IV) tetraethanolate; In tetrahydrofuran; N,N-dimethyl-formamide; acetone;

Reference yield:

: 847756-88-1
(3-chloro-4-(trifluoromethyl)phenyl)boronic acid

: 1267688-22-1
(R,R)-2-methyl-propane-2-sulfinic acid [2-[6-(3-chloro-4-trifluoromethyl-phenyl)pyrimidin-4-ylamino]-1-(4-fluoro-phenyl)-ethyl]-amide

Guidance literature:: Multi-step reaction with 2 steps

1: potassium phosphate / triphenylphosphine; palladium diacetate / acetonitrile; water / 2 h / 20 °C / Inert atmosphere

2: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 16 h / 80 °C / Inert atmosphere

With potassium phosphate; N-ethyl-N,N-diisopropylamine; palladium diacetate; triphenylphosphine; In water; N,N-dimethyl-formamide; acetonitrile;