3-((1-(5-(2-phenoxypyrimidine-4-carboxamido)pyridin-2-yl)piperidin-4-yl)methoxy)benzoic acid

Base Information

Chemical Name:3-((1-(5-(2-phenoxypyrimidine-4-carboxamido)pyridin-2-yl)piperidin-4-yl)methoxy)benzoic acid
CAS No.:1360802-00-1
Molecular Formula:C₂₉H₂₇N₅O₅
Molecular Weight:525.564
Hs Code.:

Synonyms:3-((1-(5-(2-phenoxypyrimidine-4-carboxamido)pyridin-2-yl)piperidin-4-yl)methoxy)benzoic acid

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Chemical Property of 3-((1-(5-(2-phenoxypyrimidine-4-carboxamido)pyridin-2-yl)piperidin-4-yl)methoxy)benzoic acid

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Technology Process of 3-((1-(5-(2-phenoxypyrimidine-4-carboxamido)pyridin-2-yl)piperidin-4-yl)methoxy)benzoic acid

There total 7 articles about 3-((1-(5-(2-phenoxypyrimidine-4-carboxamido)pyridin-2-yl)piperidin-4-yl)methoxy)benzoic acid 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:

: 1360801-99-5
methyl 3-((1-(5-(2-phenoxypyrimidine-4-carboxamido)pyridin-2-yl)piperidin-4-yl)methoxy)benzoate

: 1360802-00-1
3-((1-(5-(2-phenoxypyrimidine-4-carboxamido)pyridin-2-yl)piperidin-4-yl)methoxy)benzoic acid

Guidance literature:: methyl 3-((1-(5-(2-phenoxypyrimidine-4-carboxamido)pyridin-2-yl)piperidin-4-yl)methoxy)benzoate; With lithium hydroxide monohydrate; water; In tetrahydrofuran; methanol; at 20 ℃; for 16h;

With hydrogenchloride; In tetrahydrofuran; methanol; water;

Reference yield:

: 4548-45-2
2-chloro-5-nitropyridine

: 1360802-00-1
3-((1-(5-(2-phenoxypyrimidine-4-carboxamido)pyridin-2-yl)piperidin-4-yl)methoxy)benzoic acid

Guidance literature:: Multi-step reaction with 6 steps

1.1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 4 h / 100 °C

2.1: triethylamine / dichloromethane / 1.25 h / 0 - 20 °C

3.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.25 h / 20 °C / Inert atmosphere

3.2: 5 h / 50 °C

4.1: hydrogen / platinum(IV) oxide / ethyl acetate; isopropyl alcohol / 16 h / 20 °C / Inert atmosphere

5.1: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 48 h / 20 °C

6.1: water; lithium hydroxide monohydrate / tetrahydrofuran; methanol / 16 h / 20 °C

With lithium hydroxide monohydrate; water; hydrogen; sodium hydride; triethylamine; N-ethyl-N,N-diisopropylamine; HATU; platinum(IV) oxide; In tetrahydrofuran; methanol; dichloromethane; ethyl acetate; N,N-dimethyl-formamide; isopropyl alcohol; mineral oil;

Reference yield:

: 1227935-28-5
(1-(5-nitropyridin-2-yl)piperidin-4-yl)methyl methanesulfonate

: 1360802-00-1
3-((1-(5-(2-phenoxypyrimidine-4-carboxamido)pyridin-2-yl)piperidin-4-yl)methoxy)benzoic acid

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.25 h / 20 °C / Inert atmosphere

1.2: 5 h / 50 °C

2.1: hydrogen / platinum(IV) oxide / ethyl acetate; isopropyl alcohol / 16 h / 20 °C / Inert atmosphere

3.1: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 48 h / 20 °C

4.1: water; lithium hydroxide monohydrate / tetrahydrofuran; methanol / 16 h / 20 °C

With lithium hydroxide monohydrate; water; hydrogen; sodium hydride; N-ethyl-N,N-diisopropylamine; HATU; platinum(IV) oxide; In tetrahydrofuran; methanol; ethyl acetate; N,N-dimethyl-formamide; isopropyl alcohol; mineral oil;