(1'S,3R,6S)-3-[(4-benzyloxyphenyl)-(4-fluorophenylamino)-methyl]-6-(4-fluorophenyl)-tetrahydro-2H-pyran-2-one

Base Information

Chemical Name:(1'S,3R,6S)-3-[(4-benzyloxyphenyl)-(4-fluorophenylamino)-methyl]-6-(4-fluorophenyl)-tetrahydro-2H-pyran-2-one
CAS No.:1416263-36-9
Molecular Formula:C₃₁H₂₇F₂NO₃
Molecular Weight:499.557
Hs Code.:

Synonyms:(1'S,3R,6S)-3-[(4-benzyloxyphenyl)-(4-fluorophenylamino)-methyl]-6-(4-fluorophenyl)-tetrahydro-2H-pyran-2-one

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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 (1'S,3R,6S)-3-[(4-benzyloxyphenyl)-(4-fluorophenylamino)-methyl]-6-(4-fluorophenyl)-tetrahydro-2H-pyran-2-one

Chemical Property:

Purity/Quality:: HPLC ≥ 98% ^*data from raw suppliers

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Technology Process of (1'S,3R,6S)-3-[(4-benzyloxyphenyl)-(4-fluorophenylamino)-methyl]-6-(4-fluorophenyl)-tetrahydro-2H-pyran-2-one

There total 18 articles about (1'S,3R,6S)-3-[(4-benzyloxyphenyl)-(4-fluorophenylamino)-methyl]-6-(4-fluorophenyl)-tetrahydro-2H-pyran-2-one 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: 83.0%

: 1416263-38-1
(6S)-3-((R)-(4-(benzyloxy)phenyl)(4-fluorophenylamino)-methyl)-6-(4-fluorophenyl)-5,6-dihydro-2H-pyran-2-one

: 1416263-36-9
(1'S,3R,6S)-3-[(4-benzyloxyphenyl)-(4-fluorophenylamino)-methyl]-6-(4-fluorophenyl)-tetrahydro-2H-pyran-2-one

Guidance literature:: With platinum(IV) oxide; hydrogen; In toluene; at 20 ℃; under 750.075 Torr;
DOI:10.1021/jo400807c

Reference yield:

: 1416263-27-8
(2R)-2-(4-fluorophenyl)-3,4-dihydro-2H-pyran-4-ol

: 1416263-36-9
(1'S,3R,6S)-3-[(4-benzyloxyphenyl)-(4-fluorophenylamino)-methyl]-6-(4-fluorophenyl)-tetrahydro-2H-pyran-2-one

Guidance literature:: Multi-step reaction with 7 steps

1.1: dihydrogen peroxide; molybdenum(VI) oxide / acetonitrile / 24 h

2.1: pyridine; acetic anhydride / dichloromethane / 2 h / 20 °C

3.1: toluene / 72 h / Reflux

4.1: potassium iodide; chloro-trimethyl-silane / acetonitrile / 0.58 h / 20 °C

5.1: chloro-trimethyl-silane; 1H-imidazole / dichloromethane / 0.5 h / 20 °C

5.2: 0.25 h / 20 °C

6.1: lithium hydroxide / tetrahydrofuran; water / 18 h

7.1: triphenylphosphine; di-isopropyl azodicarboxylate / 3 h / 0 °C

With pyridine; 1H-imidazole; chloro-trimethyl-silane; di-isopropyl azodicarboxylate; dihydrogen peroxide; acetic anhydride; triphenylphosphine; potassium iodide; molybdenum(VI) oxide; lithium hydroxide; In tetrahydrofuran; dichloromethane; water; toluene; acetonitrile; 7.1: |Mitsunobu Displacement;
DOI:10.1021/jo400807c

Reference yield:

: 123-08-0,65581-83-1
4-hydroxy-benzaldehyde

: 1416263-36-9
(1'S,3R,6S)-3-[(4-benzyloxyphenyl)-(4-fluorophenylamino)-methyl]-6-(4-fluorophenyl)-tetrahydro-2H-pyran-2-one

Guidance literature:: Multi-step reaction with 7 steps

1.1: potassium carbonate; potassium iodide / tetrahydrofuran / 20 h / Reflux

2.1: methanesulfonic acid / acetone / 2 h / 20 °C

3.1: toluene / 72 h / Reflux

4.1: potassium iodide; chloro-trimethyl-silane / acetonitrile / 0.58 h / 20 °C

5.1: chloro-trimethyl-silane; 1H-imidazole / dichloromethane / 0.5 h / 20 °C

5.2: 0.25 h / 20 °C

6.1: lithium hydroxide / tetrahydrofuran; water / 18 h

7.1: triphenylphosphine; di-isopropyl azodicarboxylate / 3 h / 0 °C

With 1H-imidazole; chloro-trimethyl-silane; methanesulfonic acid; di-isopropyl azodicarboxylate; potassium carbonate; triphenylphosphine; potassium iodide; lithium hydroxide; In tetrahydrofuran; dichloromethane; water; acetone; toluene; acetonitrile; 7.1: |Mitsunobu Displacement;
DOI:10.1021/jo400807c