(S)-4-benzyl-3-((R)-2-((S)-(6-chloropyridin-3-yl)(hydroxy)methyl)hex-5-ynoyl)oxazolidin-2-one

Base Information

Chemical Name:(S)-4-benzyl-3-((R)-2-((S)-(6-chloropyridin-3-yl)(hydroxy)methyl)hex-5-ynoyl)oxazolidin-2-one
CAS No.:1190614-96-0
Molecular Formula:C₂₂H₂₁ClN₂O₄
Molecular Weight:412.873
Hs Code.:
Mol file:1190614-96-0.mol

Synonyms:(S)-4-benzyl-3-((R)-2-((S)-(6-chloropyridin-3-yl)(hydroxy)methyl)hex-5-ynoyl)oxazolidin-2-one

Suppliers and Price of (S)-4-benzyl-3-((R)-2-((S)-(6-chloropyridin-3-yl)(hydroxy)methyl)hex-5-ynoyl)oxazolidin-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 (S)-4-benzyl-3-((R)-2-((S)-(6-chloropyridin-3-yl)(hydroxy)methyl)hex-5-ynoyl)oxazolidin-2-one

Chemical Property:

Purity/Quality:: 99% ^*data from raw suppliers

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Technology Process of (S)-4-benzyl-3-((R)-2-((S)-(6-chloropyridin-3-yl)(hydroxy)methyl)hex-5-ynoyl)oxazolidin-2-one

There total 5 articles about (S)-4-benzyl-3-((R)-2-((S)-(6-chloropyridin-3-yl)(hydroxy)methyl)hex-5-ynoyl)oxazolidin-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: 88.0%

: 23100-12-1
6-chloronicotinylaldehyde

: 1190614-95-9
(4S)-3-hex-5-ynoyl-4-benzyl-1,3-oxazolidin-2-one

: 1190614-96-0
(S)-4-benzyl-3-((R)-2-((S)-(6-chloropyridin-3-yl)(hydroxy)methyl)hex-5-ynoyl)oxazolidin-2-one

Guidance literature:: 6-chloronicotinylaldehyde; (4S)-3-hex-5-ynoyl-4-benzyl-1,3-oxazolidin-2-one; With chloro-trimethyl-silane; triethylamine; magnesium chloride; In ethyl acetate; at 20 ℃; for 72h; Inert atmosphere;

With trifluoroacetic acid; In methanol; at 20 ℃; for 5h; Inert atmosphere;

Reference yield:

: 53293-00-8
hex-5-ynoic acid

: 1190614-96-0
(S)-4-benzyl-3-((R)-2-((S)-(6-chloropyridin-3-yl)(hydroxy)methyl)hex-5-ynoyl)oxazolidin-2-one

Guidance literature:: Multi-step reaction with 3 steps

1.1: triethylamine; pivaloyl chloride / tetrahydrofuran / 2.33 h / -25 °C / Inert atmosphere

1.2: 12 h / -25 - 20 °C

2.1: triethylamine; magnesium chloride / ethyl acetate / 72 h / 20 °C / Inert atmosphere

3.1: trifluoroacetic acid; methanol / 5 h / 20 °C / Inert atmosphere

With methanol; pivaloyl chloride; triethylamine; trifluoroacetic acid; magnesium chloride; In tetrahydrofuran; ethyl acetate;

Reference yield:

: 1190614-95-9
(4S)-3-hex-5-ynoyl-4-benzyl-1,3-oxazolidin-2-one

: 1190614-96-0
(S)-4-benzyl-3-((R)-2-((S)-(6-chloropyridin-3-yl)(hydroxy)methyl)hex-5-ynoyl)oxazolidin-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine; magnesium chloride / ethyl acetate / 72 h / 20 °C / Inert atmosphere

2: trifluoroacetic acid; methanol / 5 h / 20 °C / Inert atmosphere

With methanol; triethylamine; trifluoroacetic acid; magnesium chloride; In ethyl acetate;