(R)-2-[(2R)-2r-benzothiazol-2-yldisulfanyl-4-oxo-3c-(4-oxo-pentanoylamino)-azetidin-1-yl]-3-methyl-but-3-enoic acid benzyl ester

Base Information

Chemical Name:(R)-2-[(2R)-2r-benzothiazol-2-yldisulfanyl-4-oxo-3c-(4-oxo-pentanoylamino)-azetidin-1-yl]-3-methyl-but-3-enoic acid benzyl ester
CAS No.:67471-84-5
Molecular Formula:C₂₇H₂₇N₃O₅S₃
Molecular Weight:569.726
Hs Code.:

(<i>R</i>)-2-[(2<i>R</i>)-2<i>r</i>-benzothiazol-2-yldisulfanyl-4-oxo-3<i>c</i>-(4-oxo-pentanoylamino)-azetidin-1-yl]-3-methyl-but-3-enoic acid benzyl ester

Synonyms:(R)-2-[(2R)-2r-benzothiazol-2-yldisulfanyl-4-oxo-3c-(4-oxo-pentanoylamino)-azetidin-1-yl]-3-methyl-but-3-enoic acid benzyl ester

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Chemical Property of (R)-2-[(2R)-2r-benzothiazol-2-yldisulfanyl-4-oxo-3c-(4-oxo-pentanoylamino)-azetidin-1-yl]-3-methyl-but-3-enoic acid benzyl ester

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Technology Process of (R)-2-[(2R)-2r-benzothiazol-2-yldisulfanyl-4-oxo-3c-(4-oxo-pentanoylamino)-azetidin-1-yl]-3-methyl-but-3-enoic acid benzyl ester

There total 3 articles about (R)-2-[(2R)-2r-benzothiazol-2-yldisulfanyl-4-oxo-3c-(4-oxo-pentanoylamino)-azetidin-1-yl]-3-methyl-but-3-enoic acid benzyl 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:

: 3956-31-8,49626-54-2,64519-71-7
benzyl (2S,5R,6R)-6-amino-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate

: 67471-84-5
(R)-2-[(2R)-2r-benzothiazol-2-yldisulfanyl-4-oxo-3c-(4-oxo-pentanoylamino)-azetidin-1-yl]-3-methyl-but-3-enoic acid benzyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: ClCO₂Et / tetrahydrofuran / -18 °C

2: MCPBA / CH₂Cl₂ / -78 °C

3: (thermolysis)

With chloroformic acid ethyl ester; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; dichloromethane;
DOI:10.1021/ja00482a048

Reference yield:

: 67471-83-4
6β-(4-oxo-pentanoylamino)-penicillanic acid benzyl ester

: 67471-84-5
(R)-2-[(2R)-2r-benzothiazol-2-yldisulfanyl-4-oxo-3c-(4-oxo-pentanoylamino)-azetidin-1-yl]-3-methyl-but-3-enoic acid benzyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: MCPBA / CH₂Cl₂ / -78 °C

2: (thermolysis)

With 3-chloro-benzenecarboperoxoic acid; In dichloromethane;
DOI:10.1021/ja00482a048

Reference yield:

: 123-76-2
levulinic acid

: 67471-84-5
(R)-2-[(2R)-2r-benzothiazol-2-yldisulfanyl-4-oxo-3c-(4-oxo-pentanoylamino)-azetidin-1-yl]-3-methyl-but-3-enoic acid benzyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: ClCO₂Et / tetrahydrofuran / -18 °C

2: MCPBA / CH₂Cl₂ / -78 °C

3: (thermolysis)

With chloroformic acid ethyl ester; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; dichloromethane;
DOI:10.1021/ja00482a048