(4-(4-chlorophenyl)-5-(4-methoxyphenyl)isoxazol-3-yl)(piperidin-1-yl)methanone

Base Information

Chemical Name:(4-(4-chlorophenyl)-5-(4-methoxyphenyl)isoxazol-3-yl)(piperidin-1-yl)methanone
CAS No.:1443778-05-9
Molecular Formula:C₂₂H₂₁ClN₂O₃
Molecular Weight:396.873
Hs Code.:

Synonyms:(4-(4-chlorophenyl)-5-(4-methoxyphenyl)isoxazol-3-yl)(piperidin-1-yl)methanone

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (4-(4-chlorophenyl)-5-(4-methoxyphenyl)isoxazol-3-yl)(piperidin-1-yl)methanone

Chemical Property:

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Technology Process of (4-(4-chlorophenyl)-5-(4-methoxyphenyl)isoxazol-3-yl)(piperidin-1-yl)methanone

There total 7 articles about (4-(4-chlorophenyl)-5-(4-methoxyphenyl)isoxazol-3-yl)(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: 41.0%

: 110-89-4
piperidine

: 1443778-04-8
4-(4-chlorophenyl)-5-(4-methoxyphenyl)isoxazole-3-carboxylic acid

: 1443778-05-9
(4-(4-chlorophenyl)-5-(4-methoxyphenyl)isoxazol-3-yl)(piperidin-1-yl)methanone

Guidance literature:: With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; at 20 ℃;
DOI:10.1016/j.ejmech.2013.03.048

Reference yield:

: 1679-18-1
4-Chlorophenylboronic acid

: 1443778-05-9
(4-(4-chlorophenyl)-5-(4-methoxyphenyl)isoxazol-3-yl)(piperidin-1-yl)methanone

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium hydrogencarbonate / water; N,N-dimethyl-formamide / 0.17 h / Inert atmosphere

1.2: 3 h / 80 °C / Inert atmosphere

2.1: water; lithium hydroxide / tetrahydrofuran / 4 h / Reflux

3.1: dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 20 °C

With dmap; water; sodium hydrogencarbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; lithium hydroxide; In tetrahydrofuran; dichloromethane; water; N,N-dimethyl-formamide; 1.1: |Suzuki Coupling / 1.2: |Suzuki Coupling;
DOI:10.1016/j.ejmech.2013.03.048

Reference yield:

: 1188098-72-7
ethyl 4-bromo-5-(4-methoxyphenyl)isoxazole-3-carboxylate

: 1443778-05-9
(4-(4-chlorophenyl)-5-(4-methoxyphenyl)isoxazol-3-yl)(piperidin-1-yl)methanone

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium hydrogencarbonate / water; N,N-dimethyl-formamide / 0.17 h / Inert atmosphere

1.2: 3 h / 80 °C / Inert atmosphere

2.1: water; lithium hydroxide / tetrahydrofuran / 4 h / Reflux

3.1: dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 20 °C

With dmap; water; sodium hydrogencarbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; lithium hydroxide; In tetrahydrofuran; dichloromethane; water; N,N-dimethyl-formamide; 1.1: |Suzuki Coupling / 1.2: |Suzuki Coupling;
DOI:10.1016/j.ejmech.2013.03.048