benzyl 4-((1S,2S)-2-(2-(3-fluoro-4-(methylsulfonyl)phenoxy)ethyl)cyclopropyl)piperidine-1-carboxylate

Base Information

Chemical Name:benzyl 4-((1S,2S)-2-(2-(3-fluoro-4-(methylsulfonyl)phenoxy)ethyl)cyclopropyl)piperidine-1-carboxylate
CAS No.:1588945-00-9
Molecular Formula:C₂₅H₃₀FNO₅S
Molecular Weight:475.581
Hs Code.:

Synonyms:benzyl 4-((1S,2S)-2-(2-(3-fluoro-4-(methylsulfonyl)phenoxy)ethyl)cyclopropyl)piperidine-1-carboxylate

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Chemical Property of benzyl 4-((1S,2S)-2-(2-(3-fluoro-4-(methylsulfonyl)phenoxy)ethyl)cyclopropyl)piperidine-1-carboxylate

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Technology Process of benzyl 4-((1S,2S)-2-(2-(3-fluoro-4-(methylsulfonyl)phenoxy)ethyl)cyclopropyl)piperidine-1-carboxylate

There total 5 articles about benzyl 4-((1S,2S)-2-(2-(3-fluoro-4-(methylsulfonyl)phenoxy)ethyl)cyclopropyl)piperidine-1-carboxylate 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: 85.0%

: 859538-50-4
3-fluoro-4-(methanesulfonyl)phenol

: 1588944-70-0
benzyl 4-((1S,2S)-2-(2-hydroxyethyl)cyclopropyl)piperidine-1-carboxylate

: 1588945-00-9
benzyl 4-((1S,2S)-2-(2-(3-fluoro-4-(methylsulfonyl)phenoxy)ethyl)cyclopropyl)piperidine-1-carboxylate

Guidance literature:: With di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; at 0 - 20 ℃; for 2h; Inert atmosphere;

Reference yield:

: 369-34-6
3,4-difluoronitrobenzene

: 1588945-00-9
benzyl 4-((1S,2S)-2-(2-(3-fluoro-4-(methylsulfonyl)phenoxy)ethyl)cyclopropyl)piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 5 steps

1.1: dimethyl sulfoxide / 20 °C / Microwave irradiation

2.1: water; iron; acetic acid / 2 h / 20 °C

3.1: water; sulfuric acid; sodium nitrite / tetrahydrofuran / 1 h / 0 °C

3.2: 0.25 h / 0 °C

4.1: Oxone / water / 2 h / 20 °C

5.1: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 2 h / 0 - 20 °C / Inert atmosphere

With Oxone; di-isopropyl azodicarboxylate; sulfuric acid; water; iron; acetic acid; triphenylphosphine; sodium nitrite; In tetrahydrofuran; water; dimethyl sulfoxide;

Reference yield:

: 372121-91-0
(2-fluoro-4-nitrophenyl)(methyl)sulfone

: 1588945-00-9
benzyl 4-((1S,2S)-2-(2-(3-fluoro-4-(methylsulfonyl)phenoxy)ethyl)cyclopropyl)piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1.1: water; iron; acetic acid / 2 h / 20 °C

2.1: water; sulfuric acid; sodium nitrite / tetrahydrofuran / 1 h / 0 °C

2.2: 0.25 h / 0 °C

3.1: Oxone / water / 2 h / 20 °C

4.1: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 2 h / 0 - 20 °C / Inert atmosphere

With Oxone; di-isopropyl azodicarboxylate; sulfuric acid; water; iron; acetic acid; triphenylphosphine; sodium nitrite; In tetrahydrofuran; water;