(5R)-3-[4-(1,1-dioxo-3,6-dihydro-2H-thiopyran-4-yl)-3-fluorophenyl]-5-[(4-(hydroxymethyl)-1,2,3-triazol-1-yl)methyl]oxazolidin-2-one

Base Information

Chemical Name:(5R)-3-[4-(1,1-dioxo-3,6-dihydro-2H-thiopyran-4-yl)-3-fluorophenyl]-5-[(4-(hydroxymethyl)-1,2,3-triazol-1-yl)methyl]oxazolidin-2-one
CAS No.:591253-26-8
Molecular Formula:C₁₈H₁₉FN₄O₅S
Molecular Weight:422.437
Hs Code.:

Synonyms:(5R)-3-[4-(1,1-dioxo-3,6-dihydro-2H-thiopyran-4-yl)-3-fluorophenyl]-5-[(4-(hydroxymethyl)-1,2,3-triazol-1-yl)methyl]oxazolidin-2-one

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Chemical Property of (5R)-3-[4-(1,1-dioxo-3,6-dihydro-2H-thiopyran-4-yl)-3-fluorophenyl]-5-[(4-(hydroxymethyl)-1,2,3-triazol-1-yl)methyl]oxazolidin-2-one

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Technology Process of (5R)-3-[4-(1,1-dioxo-3,6-dihydro-2H-thiopyran-4-yl)-3-fluorophenyl]-5-[(4-(hydroxymethyl)-1,2,3-triazol-1-yl)methyl]oxazolidin-2-one

There total 2 articles about (5R)-3-[4-(1,1-dioxo-3,6-dihydro-2H-thiopyran-4-yl)-3-fluorophenyl]-5-[(4-(hydroxymethyl)-1,2,3-triazol-1-yl)methyl]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: 50.0%

: 63068-00-8
2-(phenylsulfonyl)-2-propenyl alcohol

: 591231-86-6
(5R)-3-[4-(1,1-dioxo-3,6-dihydro-2H-thiopyran-4-yl)-3-fluorophenyl]-5-(azidomethyl)oxazolidin-2-one

: (5R)-3-[4-(1,1-dioxo-3,6-dihydro-2H-thiopyran-4-yl)-3-fluorophenyl]-5-[(5-hydroxymethyl-1,2,3-triazol-1-yl)methyl]oxazolidin-2-one

: 591253-26-8
(5R)-3-[4-(1,1-dioxo-3,6-dihydro-2H-thiopyran-4-yl)-3-fluorophenyl]-5-[(4-(hydroxymethyl)-1,2,3-triazol-1-yl)methyl]oxazolidin-2-one

Guidance literature:: With 1-methyl-pyrrolidin-2-one; at 90 ℃; for 4h;
DOI:10.1021/jm0400810

Reference yield:

: 371195-52-7
(5R)-3-[4-(3,6-dihydro-2H-thiopyran-4-yl)-3-fluorophenyl]-5-azidomethyloxazolidin-2-one

: 591253-26-8
(5R)-3-[4-(1,1-dioxo-3,6-dihydro-2H-thiopyran-4-yl)-3-fluorophenyl]-5-[(4-(hydroxymethyl)-1,2,3-triazol-1-yl)methyl]oxazolidin-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: 88 percent / 3-chloroperbenzoic acid / CH₂Cl₂ / 2.5 h / 0 - 20 °C

2: 50 percent / N-methylpyrrolidone / 4 h / 90 °C

With 1-methyl-pyrrolidin-2-one; 3-chloro-benzenecarboperoxoic acid; In dichloromethane;
DOI:10.1021/jm0400810

Reference yield: 84.0%

: 79-37-8
oxalyl dichloride

: 591253-26-8
(5R)-3-[4-(1,1-dioxo-3,6-dihydro-2H-thiopyran-4-yl)-3-fluorophenyl]-5-[(4-(hydroxymethyl)-1,2,3-triazol-1-yl)methyl]oxazolidin-2-one

: 591253-50-8
(5R)-3-[4-(1,1-dioxo-3,6-dihydro-2H-thiopyran-4-yl)-3-fluorophenyl]-5-[4-carboxaldehyde-1,2,3-triazol-1-ylmethyl]oxazolidin-2-one

Guidance literature:: oxalyl dichloride; With dimethyl sulfoxide; In dichloromethane; at -50 ℃; for 0.166667h;

(5R)-3-[4-(1,1-dioxo-3,6-dihydro-2H-thiopyran-4-yl)-3-fluorophenyl]-5-[(4-(hydroxymethyl)-1,2,3-triazol-1-yl)methyl]oxazolidin-2-one; In 1-methyl-pyrrolidin-2-one; dichloromethane; at -50 ℃; for 1h;

With N-ethyl-N,N-diisopropylamine; In 1-methyl-pyrrolidin-2-one; dichloromethane; at -50 - -20 ℃;