(S)-N-{3-[3-fluoro-4-(4-oxo-4-prop-2-ynyloxy-4λ5-[1,4]azaphosphinan-1-yl)-phenyl]-2-oxo-oxazolidin-5-ylmethyl}-acetamide

Base Information

Chemical Name:(S)-N-{3-[3-fluoro-4-(4-oxo-4-prop-2-ynyloxy-4λ5-[1,4]azaphosphinan-1-yl)-phenyl]-2-oxo-oxazolidin-5-ylmethyl}-acetamide
CAS No.:1042425-04-6
Molecular Formula:C₁₉H₂₃FN₃O₅P
Molecular Weight:423.381
Hs Code.:

Synonyms:(S)-N-{3-[3-fluoro-4-(4-oxo-4-prop-2-ynyloxy-4λ5-[1,4]azaphosphinan-1-yl)-phenyl]-2-oxo-oxazolidin-5-ylmethyl}-acetamide

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Chemical Property of (S)-N-{3-[3-fluoro-4-(4-oxo-4-prop-2-ynyloxy-4λ5-[1,4]azaphosphinan-1-yl)-phenyl]-2-oxo-oxazolidin-5-ylmethyl}-acetamide

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Technology Process of (S)-N-{3-[3-fluoro-4-(4-oxo-4-prop-2-ynyloxy-4λ5-[1,4]azaphosphinan-1-yl)-phenyl]-2-oxo-oxazolidin-5-ylmethyl}-acetamide

There total 8 articles about (S)-N-{3-[3-fluoro-4-(4-oxo-4-prop-2-ynyloxy-4λ5-[1,4]azaphosphinan-1-yl)-phenyl]-2-oxo-oxazolidin-5-ylmethyl}-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: 50.3%

: 1042425-00-2
(S)-N-{3-[3-fluoro-4-(4-hydroxy-4-oxo-4λ5-[1,4]azaphosphinan-1-yl)-phenyl]-2-oxo-oxazolidin-5-ylmethyl }-acetamide

: 106-96-7
propargyl bromide

: 1042425-04-6
(S)-N-{3-[3-fluoro-4-(4-oxo-4-prop-2-ynyloxy-4λ5-[1,4]azaphosphinan-1-yl)-phenyl]-2-oxo-oxazolidin-5-ylmethyl}-acetamide

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; toluene; for 36h; Heating / reflux;

Reference yield:

: 1042425-94-4
4-ethoxy-1-(2-fluoro-4-nitro-phenyl)-[1,4]azaphosphinane 4-oxide

: 1042425-04-6
(S)-N-{3-[3-fluoro-4-(4-oxo-4-prop-2-ynyloxy-4λ5-[1,4]azaphosphinan-1-yl)-phenyl]-2-oxo-oxazolidin-5-ylmethyl}-acetamide

Guidance literature:: Multi-step reaction with 8 steps

1.1: hydrogen / palladium 10% on activated carbon / methanol / 3 h / 20 °C

2.1: sodium hydrogencarbonate / water; acetone; toluene / 2 h / 0 °C

3.1: n-butyllithium / tetrahydrofuran / 1 h / -78 °C

3.2: 13 h / -78 - 20 °C

4.1: triethylamine / dichloromethane / 1.17 h / 0 - 20 °C

5.1: sodium azide / N,N-dimethyl-formamide / 2 h / 80 °C

6.1: 15 h / 20 °C

7.1: trimethylsilyl bromide / dichloromethane / 12 h / 40 °C

7.2: 1 h

8.1: potassium carbonate / N,N-dimethyl-formamide; toluene / 36 h / Heating / reflux

With n-butyllithium; sodium azide; trimethylsilyl bromide; hydrogen; sodium hydrogencarbonate; potassium carbonate; triethylamine; palladium 10% on activated carbon; In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide; acetone; toluene;

Reference yield:

: 1042425-95-5
4-(4-ethoxy-4-oxo-4λ5-[1,4]azaphosphinan-1-yl)-3-fluoro-phenyl-amine

: 1042425-04-6
(S)-N-{3-[3-fluoro-4-(4-oxo-4-prop-2-ynyloxy-4λ5-[1,4]azaphosphinan-1-yl)-phenyl]-2-oxo-oxazolidin-5-ylmethyl}-acetamide

Guidance literature:: Multi-step reaction with 7 steps

1.1: sodium hydrogencarbonate / water; acetone; toluene / 2 h / 0 °C

2.1: n-butyllithium / tetrahydrofuran / 1 h / -78 °C

2.2: 13 h / -78 - 20 °C

3.1: triethylamine / dichloromethane / 1.17 h / 0 - 20 °C

4.1: sodium azide / N,N-dimethyl-formamide / 2 h / 80 °C

5.1: 15 h / 20 °C

6.1: trimethylsilyl bromide / dichloromethane / 12 h / 40 °C

6.2: 1 h

7.1: potassium carbonate / N,N-dimethyl-formamide; toluene / 36 h / Heating / reflux

With n-butyllithium; sodium azide; trimethylsilyl bromide; sodium hydrogencarbonate; potassium carbonate; triethylamine; In tetrahydrofuran; dichloromethane; water; N,N-dimethyl-formamide; acetone; toluene;