(R)-1-[(2R,5R)-2-Benzhydryl-5-(4-fluoro-benzylamino)-piperidin-1-yl]-2-methoxy-2-phenyl-ethanone

Base Information

Chemical Name:(R)-1-[(2R,5R)-2-Benzhydryl-5-(4-fluoro-benzylamino)-piperidin-1-yl]-2-methoxy-2-phenyl-ethanone
CAS No.:546095-43-6
Molecular Formula:C₃₄H₃₅FN₂O₂
Molecular Weight:522.663
Hs Code.:

Synonyms:(R)-1-[(2R,5R)-2-Benzhydryl-5-(4-fluoro-benzylamino)-piperidin-1-yl]-2-methoxy-2-phenyl-ethanone

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Chemical Property of (R)-1-[(2R,5R)-2-Benzhydryl-5-(4-fluoro-benzylamino)-piperidin-1-yl]-2-methoxy-2-phenyl-ethanone

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Technology Process of (R)-1-[(2R,5R)-2-Benzhydryl-5-(4-fluoro-benzylamino)-piperidin-1-yl]-2-methoxy-2-phenyl-ethanone

There total 7 articles about (R)-1-[(2R,5R)-2-Benzhydryl-5-(4-fluoro-benzylamino)-piperidin-1-yl]-2-methoxy-2-phenyl-ethanone 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:

: N-(6-benzhydrylpyridin-3-yl)acetamide dihydrochloride

: 546095-43-6
(R)-1-[(2R,5R)-2-Benzhydryl-5-(4-fluoro-benzylamino)-piperidin-1-yl]-2-methoxy-2-phenyl-ethanone

Guidance literature:: Multi-step reaction with 5 steps

1: 48 percent / H₂ / PtO₂ / methanol / 12 h / 20 °C / 3102.89 Torr

2: 43 percent / Et₃N / CH₂Cl₂ / 12 h

3: 70 percent / aq. HCl / methanol / Heating

4: AcOH / 1,2-dichloro-ethane

5: NaBH₃CN / 1,2-dichloro-ethane; methanol

With hydrogenchloride; hydrogen; sodium cyanoborohydride; acetic acid; triethylamine; platinum(IV) oxide; In methanol; dichloromethane; 1,2-dichloro-ethane;
DOI:10.1021/jm020561w

Reference yield:

: (R)-1-((2R,5R)-2-Benzhydryl-5-{[1-(4-fluoro-phenyl)-meth-(E)-ylidene]-amino}-piperidin-1-yl)-2-methoxy-2-phenyl-ethanone

: 546095-43-6
(R)-1-[(2R,5R)-2-Benzhydryl-5-(4-fluoro-benzylamino)-piperidin-1-yl]-2-methoxy-2-phenyl-ethanone

Guidance literature:: With sodium cyanoborohydride; In methanol; 1,2-dichloro-ethane;
DOI:10.1021/jm020561w

Reference yield:

: 34713-98-9
(R)-(-)-α-methoxyphenylacetyl chloride

: 546095-43-6
(R)-1-[(2R,5R)-2-Benzhydryl-5-(4-fluoro-benzylamino)-piperidin-1-yl]-2-methoxy-2-phenyl-ethanone

Guidance literature:: Multi-step reaction with 4 steps

1: 43 percent / Et₃N / CH₂Cl₂ / 12 h

2: 70 percent / aq. HCl / methanol / Heating

3: AcOH / 1,2-dichloro-ethane

4: NaBH₃CN / 1,2-dichloro-ethane; methanol

With hydrogenchloride; sodium cyanoborohydride; acetic acid; triethylamine; In methanol; dichloromethane; 1,2-dichloro-ethane;
DOI:10.1021/jm020561w