1-[4-[4-[(5R)-4,5-dihydro-5-phenyl-3-isoxazolyl]-2-thiazolyl]-1-piperidinyl]-N-[2,5-dimethylphenyl]carboxamide

Base Information

Chemical Name:1-[4-[4-[(5R)-4,5-dihydro-5-phenyl-3-isoxazolyl]-2-thiazolyl]-1-piperidinyl]-N-[2,5-dimethylphenyl]carboxamide
CAS No.:1148044-99-8
Molecular Formula:C₂₆H₂₈N₄O₂S
Molecular Weight:460.6
Hs Code.:

Synonyms:1-[4-[4-[(5R)-4,5-dihydro-5-phenyl-3-isoxazolyl]-2-thiazolyl]-1-piperidinyl]-N-[2,5-dimethylphenyl]carboxamide

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Chemical Property of 1-[4-[4-[(5R)-4,5-dihydro-5-phenyl-3-isoxazolyl]-2-thiazolyl]-1-piperidinyl]-N-[2,5-dimethylphenyl]carboxamide

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Technology Process of 1-[4-[4-[(5R)-4,5-dihydro-5-phenyl-3-isoxazolyl]-2-thiazolyl]-1-piperidinyl]-N-[2,5-dimethylphenyl]carboxamide

There total 10 articles about 1-[4-[4-[(5R)-4,5-dihydro-5-phenyl-3-isoxazolyl]-2-thiazolyl]-1-piperidinyl]-N-[2,5-dimethylphenyl]carboxamide 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:

: 1003320-28-2
2-bromo-1-[(5R)-4,5-dihydro-5-phenyl-3-isoxazolyl]ethanone

: 1148046-80-3
4-(aminothioxomethyl)-N-(2,5-dimethylphenyl)-1-piperidinecarboxamide

: 1148044-99-8
1-[4-[4-[(5R)-4,5-dihydro-5-phenyl-3-isoxazolyl]-2-thiazolyl]-1-piperidinyl]-N-[2,5-dimethylphenyl]carboxamide

Guidance literature:: In acetone; at 45 ℃;

Reference yield:

: (5R)-4,5-dihydro-5-phenyl-3-isoxazole-carboxylic acid cinchonine salt

: 1148044-99-8
1-[4-[4-[(5R)-4,5-dihydro-5-phenyl-3-isoxazolyl]-2-thiazolyl]-1-piperidinyl]-N-[2,5-dimethylphenyl]carboxamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: hydrogenchloride / ethyl acetate; cyclohexane

2.1: thionyl chloride / N,N-dimethyl-formamide / ethyl acetate / 3 h / 20 °C / Reflux

2.2: 5 - 10 °C

3.1: toluene; tetrahydrofuran / 1 h / -15 °C

4.1: bromine / 1,2-dichloro-ethane / 0.5 h / 30 °C

5.1: acetone / 17 h / 45 °C / vortexed

5.2: 1 h / 20 °C

With hydrogenchloride; thionyl chloride; bromine; N,N-dimethyl-formamide; In tetrahydrofuran; cyclohexane; ethyl acetate; 1,2-dichloro-ethane; acetone; toluene;

Reference yield:

: 100-42-5,25038-60-2,25247-68-1,28213-80-1,28325-75-9,79637-11-9,9003-53-6
styrene

: 1148044-99-8
1-[4-[4-[(5R)-4,5-dihydro-5-phenyl-3-isoxazolyl]-2-thiazolyl]-1-piperidinyl]-N-[2,5-dimethylphenyl]carboxamide

Guidance literature:: Multi-step reaction with 8 steps

1.1: potassium hydrogencarbonate / toluene; water / 1 h / 7 - 10 °C

2.1: sodium hydroxide; water / methanol / 20 - 45 °C

2.2: pH ~ 1

3.1: hydrocinchonidine / methanol / 20 - 57 °C

4.1: hydrogenchloride / ethyl acetate; cyclohexane

5.1: thionyl chloride / N,N-dimethyl-formamide / ethyl acetate / 3 h / 20 °C / Reflux

5.2: 5 - 10 °C

6.1: toluene; tetrahydrofuran / 1 h / -15 °C

7.1: bromine / 1,2-dichloro-ethane / 0.5 h / 30 °C

8.1: acetone / 17 h / 45 °C / vortexed

8.2: 1 h / 20 °C

With hydrogenchloride; thionyl chloride; water; bromine; potassium hydrogencarbonate; sodium hydroxide; hydrocinchonidine; N,N-dimethyl-formamide; In tetrahydrofuran; methanol; cyclohexane; water; ethyl acetate; 1,2-dichloro-ethane; acetone; toluene;