(R)-(2-cyclopropyl-5-m-tolyl-thiazol-4-yl)-[3-(4-trifluoromethyl-pyrimidin-2-ylamino)-piperidin-1-yl]-methanone

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Chemical Name:(R)-(2-cyclopropyl-5-m-tolyl-thiazol-4-yl)-[3-(4-trifluoromethyl-pyrimidin-2-ylamino)-piperidin-1-yl]-methanone
CAS No.:1193495-61-2
Molecular Formula:C₂₄H₂₄F₃N₅OS
Molecular Weight:487.549
Hs Code.:

Synonyms:(R)-(2-cyclopropyl-5-m-tolyl-thiazol-4-yl)-[3-(4-trifluoromethyl-pyrimidin-2-ylamino)-piperidin-1-yl]-methanone

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Chemical Property of (R)-(2-cyclopropyl-5-m-tolyl-thiazol-4-yl)-[3-(4-trifluoromethyl-pyrimidin-2-ylamino)-piperidin-1-yl]-methanone

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Technology Process of (R)-(2-cyclopropyl-5-m-tolyl-thiazol-4-yl)-[3-(4-trifluoromethyl-pyrimidin-2-ylamino)-piperidin-1-yl]-methanone

There total 5 articles about (R)-(2-cyclopropyl-5-m-tolyl-thiazol-4-yl)-[3-(4-trifluoromethyl-pyrimidin-2-ylamino)-piperidin-1-yl]-methanone 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:

: (R)-(3-amino-piperidin-1-yl)-(2-cyclopropyl-5-m-tolyl-thiazol-4-yl)-methanone dihydrochloride

: 33034-67-2
2-chloro-4-trifluoromethylpyrimidine

: 1193495-61-2
(R)-(2-cyclopropyl-5-m-tolyl-thiazol-4-yl)-[3-(4-trifluoromethyl-pyrimidin-2-ylamino)-piperidin-1-yl]-methanone

Guidance literature:: With potassium carbonate; N-ethyl-N,N-diisopropylamine; In o-xylene; at 145 ℃; for 16h;

Reference yield:

: 620-23-5
m-tolyl aldehyde

: 1193495-61-2
(R)-(2-cyclopropyl-5-m-tolyl-thiazol-4-yl)-[3-(4-trifluoromethyl-pyrimidin-2-ylamino)-piperidin-1-yl]-methanone

Guidance literature:: Multi-step reaction with 6 steps

1.1: potassium tert-butylate / tetrahydrofuran / -60 - 20 °C

2.1: acetonitrile / 5 h / Molecular sieve

2.2: 6 h / 50 °C

3.1: sodium hydroxide; water / isopropyl alcohol; tetrahydrofuran

3.2: pH 3 - 4

4.1: N-ethyl-N,N-diisopropylamine; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate / acetonitrile / 0.25 h / 20 °C

4.2: 2 h / 20 °C

5.1: hydrogenchloride / 1,4-dioxane / 1 h / 20 °C

6.1: potassium carbonate; N-ethyl-N,N-diisopropylamine / o-xylene / 16 h / 145 °C

With hydrogenchloride; potassium tert-butylate; water; potassium carbonate; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine; sodium hydroxide; In tetrahydrofuran; 1,4-dioxane; o-xylene; isopropyl alcohol; acetonitrile;

Reference yield:

: 1083282-61-4
2-cyclopropyl-5-(3-methyl-phenyl)-thiazole-4-carboxylic acid

: 1193495-61-2
(R)-(2-cyclopropyl-5-m-tolyl-thiazol-4-yl)-[3-(4-trifluoromethyl-pyrimidin-2-ylamino)-piperidin-1-yl]-methanone

Guidance literature:: Multi-step reaction with 3 steps

1.1: N-ethyl-N,N-diisopropylamine; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate / acetonitrile / 0.25 h / 20 °C

1.2: 2 h / 20 °C

2.1: hydrogenchloride / 1,4-dioxane / 1 h / 20 °C

3.1: potassium carbonate; N-ethyl-N,N-diisopropylamine / o-xylene / 16 h / 145 °C

With hydrogenchloride; potassium carbonate; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine; In 1,4-dioxane; o-xylene; acetonitrile;