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N-methoxalyl pyruvoylthio azetidinone

Base Information
  • Chemical Name:N-methoxalyl pyruvoylthio azetidinone
  • CAS No.:73933-10-5
  • Molecular Formula:C25H29N3O9S
  • Molecular Weight:547.586
  • Hs Code.:
N-methoxalyl pyruvoylthio azetidinone

Synonyms:N-methoxalyl pyruvoylthio azetidinone

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Chemical Property of N-methoxalyl pyruvoylthio azetidinone
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Technology Process of N-methoxalyl pyruvoylthio azetidinone

There total 7 articles about N-methoxalyl pyruvoylthio azetidinone 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:
Guidance literature:
Multi-step reaction with 7 steps
1: 88 percent / CH2Cl2; diethyl ether / 0.5 h / 0 °C
2: 79 percent / 90percent m-chloroperbenzoic acid / CH2Cl2 / 1.5 h / Ambient temperature
3: 56 percent / benzene / 90 h / Heating
4: 97 percent / Et3N / CH2Cl2 / 1 h / Ambient temperature
5: 89 percent / i-Pr2NEt / dioxane / 72 h / 50 °C
6: 1.) PH3P / 1.) H2O, CH2Cl2, 0 to 5 deg C, 88 h, 2.) pyridine, RT; 4.5 h
7: 93 percent / O3 / methanol / 1.67 h / -75 °C
With ozone; triethylamine; N-ethyl-N,N-diisopropylamine; 3-chloro-benzenecarboperoxoic acid; triphenylphosphine; In 1,4-dioxane; methanol; diethyl ether; dichloromethane; benzene;
DOI:10.1002/hlca.19800630119
Guidance literature:
Multi-step reaction with 6 steps
1: 79 percent / 90percent m-chloroperbenzoic acid / CH2Cl2 / 1.5 h / Ambient temperature
2: 56 percent / benzene / 90 h / Heating
3: 97 percent / Et3N / CH2Cl2 / 1 h / Ambient temperature
4: 89 percent / i-Pr2NEt / dioxane / 72 h / 50 °C
5: 1.) PH3P / 1.) H2O, CH2Cl2, 0 to 5 deg C, 88 h, 2.) pyridine, RT; 4.5 h
6: 93 percent / O3 / methanol / 1.67 h / -75 °C
With ozone; triethylamine; N-ethyl-N,N-diisopropylamine; 3-chloro-benzenecarboperoxoic acid; triphenylphosphine; In 1,4-dioxane; methanol; dichloromethane; benzene;
DOI:10.1002/hlca.19800630119
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