2-Methoxy-N-(2-methoxy-phenyl)-N-[(3S,4R)-3-methyl-1-(2-thiophen-2-yl-ethyl)-piperidin-4-yl]-acetamide

Base Information

Chemical Name:2-Methoxy-N-(2-methoxy-phenyl)-N-[(3S,4R)-3-methyl-1-(2-thiophen-2-yl-ethyl)-piperidin-4-yl]-acetamide
CAS No.:130149-98-3
Molecular Formula:C₂₂H₃₀N₂O₃S
Molecular Weight:402.558
Hs Code.:

Synonyms:2-Methoxy-N-(2-methoxy-phenyl)-N-[(3S,4R)-3-methyl-1-(2-thiophen-2-yl-ethyl)-piperidin-4-yl]-acetamide

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Chemical Property of 2-Methoxy-N-(2-methoxy-phenyl)-N-[(3S,4R)-3-methyl-1-(2-thiophen-2-yl-ethyl)-piperidin-4-yl]-acetamide

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Technology Process of 2-Methoxy-N-(2-methoxy-phenyl)-N-[(3S,4R)-3-methyl-1-(2-thiophen-2-yl-ethyl)-piperidin-4-yl]-acetamide

There total 6 articles about 2-Methoxy-N-(2-methoxy-phenyl)-N-[(3S,4R)-3-methyl-1-(2-thiophen-2-yl-ethyl)-piperidin-4-yl]-acetamide 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:

: 34737-89-8
1-Benzyl-3-methyl-4-piperidon

: 130149-98-3
2-Methoxy-N-(2-methoxy-phenyl)-N-[(3S,4R)-3-methyl-1-(2-thiophen-2-yl-ethyl)-piperidin-4-yl]-acetamide

Guidance literature:: Multi-step reaction with 5 steps

1: p-toluenesulfonic acid / toluene / Heating

2: NaBH₄ / methanol / Ambient temperature

3: CH₂Cl₂

4: H₂ / 10percent Pd(OH)2/C / ethanol / 2585.7 Torr

5: Na₂CO₃, NaI / acetonitrile

With sodium tetrahydroborate; hydrogen; sodium carbonate; toluene-4-sulfonic acid; sodium iodide; palladium dihydroxide; In methanol; ethanol; dichloromethane; toluene; acetonitrile;
DOI:10.1021/jm00172a032

Reference yield:

: 90-04-0
2-methoxy-phenylamine

: 130149-98-3
2-Methoxy-N-(2-methoxy-phenyl)-N-[(3S,4R)-3-methyl-1-(2-thiophen-2-yl-ethyl)-piperidin-4-yl]-acetamide

Guidance literature:: Multi-step reaction with 5 steps

1: p-toluenesulfonic acid / toluene / Heating

2: NaBH₄ / methanol / Ambient temperature

3: CH₂Cl₂

4: H₂ / 10percent Pd(OH)2/C / ethanol / 2585.7 Torr

5: Na₂CO₃, NaI / acetonitrile

With sodium tetrahydroborate; hydrogen; sodium carbonate; toluene-4-sulfonic acid; sodium iodide; palladium dihydroxide; In methanol; ethanol; dichloromethane; toluene; acetonitrile;
DOI:10.1021/jm00172a032

Reference yield:

: 79278-29-8
[1-Benzyl-3-methyl-piperidin-(4E)-ylidene]-(2-methoxy-phenyl)-amine

: 130149-98-3
2-Methoxy-N-(2-methoxy-phenyl)-N-[(3S,4R)-3-methyl-1-(2-thiophen-2-yl-ethyl)-piperidin-4-yl]-acetamide

Guidance literature:: Multi-step reaction with 4 steps

1: NaBH₄ / methanol / Ambient temperature

2: CH₂Cl₂

3: H₂ / 10percent Pd(OH)2/C / ethanol / 2585.7 Torr

4: Na₂CO₃, NaI / acetonitrile

With sodium tetrahydroborate; hydrogen; sodium carbonate; sodium iodide; palladium dihydroxide; In methanol; ethanol; dichloromethane; acetonitrile;
DOI:10.1021/jm00172a032