Benzoic acid (2S,5R)-5-(5-benzyl-4-methylsulfanyl-2-oxo-2H-pyrimidin-1-yl)-tetrahydro-furan-2-ylmethyl ester

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Chemical Name:Benzoic acid (2S,5R)-5-(5-benzyl-4-methylsulfanyl-2-oxo-2H-pyrimidin-1-yl)-tetrahydro-furan-2-ylmethyl ester
CAS No.:178551-11-6
Molecular Formula:C₂₄H₂₄N₂O₄S
Molecular Weight:436.532
Hs Code.:

Synonyms:Benzoic acid (2S,5R)-5-(5-benzyl-4-methylsulfanyl-2-oxo-2H-pyrimidin-1-yl)-tetrahydro-furan-2-ylmethyl ester

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Chemical Property of Benzoic acid (2S,5R)-5-(5-benzyl-4-methylsulfanyl-2-oxo-2H-pyrimidin-1-yl)-tetrahydro-furan-2-ylmethyl ester

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Technology Process of Benzoic acid (2S,5R)-5-(5-benzyl-4-methylsulfanyl-2-oxo-2H-pyrimidin-1-yl)-tetrahydro-furan-2-ylmethyl ester

There total 4 articles about Benzoic acid (2S,5R)-5-(5-benzyl-4-methylsulfanyl-2-oxo-2H-pyrimidin-1-yl)-tetrahydro-furan-2-ylmethyl ester 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%

: 178551-08-1
Benzoic acid (2S,5R)-5-(5-benzyl-2-oxo-4-thioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-2-ylmethyl ester

: 74-88-4
methyl iodide

: 178551-11-6
Benzoic acid (2S,5R)-5-(5-benzyl-4-methylsulfanyl-2-oxo-2H-pyrimidin-1-yl)-tetrahydro-furan-2-ylmethyl ester

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; for 0.5h; Ambient temperature;
DOI:10.1135/cccc19960627

Reference yield:

: 178551-07-0
Benzoic acid (2S,5R)-5-(5-benzyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-2-ylmethyl ester

: 178551-11-6
Benzoic acid (2S,5R)-5-(5-benzyl-4-methylsulfanyl-2-oxo-2H-pyrimidin-1-yl)-tetrahydro-furan-2-ylmethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 77 percent / Lawesson reagent / 1,2-dichloro-ethane / 3 h / Heating

2: 88 percent / K₂CO₃ / dimethylformamide / 0.5 h / Ambient temperature

With Lawessons reagent; potassium carbonate; In 1,2-dichloro-ethane; N,N-dimethyl-formamide;
DOI:10.1135/cccc19960627

Reference yield:

: 178551-06-9
Benzoic acid (2R,3S,5R)-5-(5-benzyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-3-hydroxy-tetrahydro-furan-2-ylmethyl ester

: 178551-11-6
Benzoic acid (2S,5R)-5-(5-benzyl-4-methylsulfanyl-2-oxo-2H-pyrimidin-1-yl)-tetrahydro-furan-2-ylmethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) SOCl₂, 2.) tributylstannane, azobis(isobutyronitrile) / 1.) HMTA, room temp., overnight, 2.) toluene, reflux, 1 h

2: 77 percent / Lawesson reagent / 1,2-dichloro-ethane / 3 h / Heating

3: 88 percent / K₂CO₃ / dimethylformamide / 0.5 h / Ambient temperature

With Lawessons reagent; thionyl chloride; 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; potassium carbonate; In 1,2-dichloro-ethane; N,N-dimethyl-formamide;
DOI:10.1135/cccc19960627