3-[1-(tert-butyldimethylsilyloxy)-1-(1-methyl-1H-1,2,3-triazol-4-yl)methyl]-4-(phenylsulfanyl)azetidin-2-one

Base Information

Chemical Name:3-[1-(tert-butyldimethylsilyloxy)-1-(1-methyl-1H-1,2,3-triazol-4-yl)methyl]-4-(phenylsulfanyl)azetidin-2-one
CAS No.:247188-87-0
Molecular Formula:C₁₉H₂₈N₄O₂SSi
Molecular Weight:404.608
Hs Code.:

Synonyms:3-[1-(tert-butyldimethylsilyloxy)-1-(1-methyl-1H-1,2,3-triazol-4-yl)methyl]-4-(phenylsulfanyl)azetidin-2-one

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Chemical Property of 3-[1-(tert-butyldimethylsilyloxy)-1-(1-methyl-1H-1,2,3-triazol-4-yl)methyl]-4-(phenylsulfanyl)azetidin-2-one

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Technology Process of 3-[1-(tert-butyldimethylsilyloxy)-1-(1-methyl-1H-1,2,3-triazol-4-yl)methyl]-4-(phenylsulfanyl)azetidin-2-one

There total 5 articles about 3-[1-(tert-butyldimethylsilyloxy)-1-(1-methyl-1H-1,2,3-triazol-4-yl)methyl]-4-(phenylsulfanyl)azetidin-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: 69.0%

: 108-98-5
thiophenol

: 247188-85-8
4-acetoxy-3-[1-(tert-butyldimethylsilyloxy)-1-(1-methyl-1H-1,2,3-triazol-4-yl)methyl]azetidin-2-one

: 247188-87-0
3-[1-(tert-butyldimethylsilyloxy)-1-(1-methyl-1H-1,2,3-triazol-4-yl)methyl]-4-(phenylsulfanyl)azetidin-2-one

Guidance literature:: With sodium hydroxide; In water; acetone; at 20 ℃; for 4h;
DOI:10.1007/BF02256811

Reference yield:

: 18162-48-6
tert-butyldimethylsilyl chloride

: 247188-87-0
3-[1-(tert-butyldimethylsilyloxy)-1-(1-methyl-1H-1,2,3-triazol-4-yl)methyl]-4-(phenylsulfanyl)azetidin-2-one

Guidance literature:: Multi-step reaction with 4 steps

1: 75 percent / imidazole / CH₂Cl₂ / 28 h / 20 °C

2: 92 percent / acetic acid / 1.5 h / 90 °C

3: 750 mg / KMnO₄; NaIO₄ / acetone; H₂O; aq. phosphate buffer / 20 °C / pH 7.0

4: 69 percent / NaOH / acetone; H₂O / 4 h / 20 °C

With 1H-imidazole; sodium hydroxide; potassium permanganate; sodium periodate; In phosphate buffer; dichloromethane; water; acetic acid; acetone; 1: Substitution / 2: Ring cleavage / 3: Oxidation / 4: Substitution;
DOI:10.1007/BF02256811

Reference yield:

: methyl 6-[1-hydroxy-1-(1-methyl-1H-1,2,3-triazol-4-yl)methyl]penicillanate

: 247188-87-0
3-[1-(tert-butyldimethylsilyloxy)-1-(1-methyl-1H-1,2,3-triazol-4-yl)methyl]-4-(phenylsulfanyl)azetidin-2-one

Guidance literature:: Multi-step reaction with 4 steps

1: 75 percent / imidazole / CH₂Cl₂ / 28 h / 20 °C

2: 92 percent / acetic acid / 1.5 h / 90 °C

3: 750 mg / KMnO₄; NaIO₄ / acetone; H₂O; aq. phosphate buffer / 20 °C / pH 7.0

4: 69 percent / NaOH / acetone; H₂O / 4 h / 20 °C

With 1H-imidazole; sodium hydroxide; potassium permanganate; sodium periodate; In phosphate buffer; dichloromethane; water; acetic acid; acetone; 1: Substitution / 2: Ring cleavage / 3: Oxidation / 4: Substitution;
DOI:10.1007/BF02256811