2-<3-phenylacetamido-4-thio(aminocarbonyl-methyl)-(3R,4R)-azetidin-2-on-1-yl>-trichloroethyl acetate

Base Information

Chemical Name:2-<3-phenylacetamido-4-thio(aminocarbonyl-methyl)-(3R,4R)-azetidin-2-on-1-yl>-trichloroethyl acetate
CAS No.:122692-28-8
Molecular Formula:C₁₇H₁₈Cl₃N₃O₅S
Molecular Weight:482.772
Hs Code.:

Synonyms:2-<3-phenylacetamido-4-thio(aminocarbonyl-methyl)-(3R,4R)-azetidin-2-on-1-yl>-trichloroethyl acetate

Suppliers and Price of 2-<3-phenylacetamido-4-thio(aminocarbonyl-methyl)-(3R,4R)-azetidin-2-on-1-yl>-trichloroethyl acetate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 2-<3-phenylacetamido-4-thio(aminocarbonyl-methyl)-(3R,4R)-azetidin-2-on-1-yl>-trichloroethyl acetate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2-<3-phenylacetamido-4-thio(aminocarbonyl-methyl)-(3R,4R)-azetidin-2-on-1-yl>-trichloroethyl acetate

There total 2 articles about 2-<3-phenylacetamido-4-thio(aminocarbonyl-methyl)-(3R,4R)-azetidin-2-on-1-yl>-trichloroethyl acetate 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: 71.0%

: 144-48-9
iodacetamide

: 122691-74-1
2-<3-phenylacetamido-4-thiol-(3R,4R)-azetidin-2-on-1-yl>-trichloroethyl acetate

: 122692-28-8
2-<3-phenylacetamido-4-thio(aminocarbonyl-methyl)-(3R,4R)-azetidin-2-on-1-yl>-trichloroethyl acetate

Guidance literature:: With triethylamine; In N,N-dimethyl-formamide; at 0 ℃; for 1h; then 20 deg C;
DOI:10.1016/0223-5234(88)90100-6

Reference yield:

: 87996-82-5
2-<3-benzyl-6-oxo-2-thia-4,7-diaza-(1R,5R)-bicyclo-<3.2.0>-hept-3-en-7-yl>-acetic acid-β-trichloroethyl ester

: 122692-28-8
2-<3-phenylacetamido-4-thio(aminocarbonyl-methyl)-(3R,4R)-azetidin-2-on-1-yl>-trichloroethyl acetate

Guidance literature:: Multi-step reaction with 2 steps

1: 80 percent / 1.2 N aq HCl / dimethylformamide / 1 h / Ambient temperature

2: 71 percent / triethylamine / dimethylformamide / 1 h / 0 °C / then 20 deg C

With hydrogenchloride; triethylamine; In N,N-dimethyl-formamide;
DOI:10.1016/0223-5234(88)90100-6

Reference yield: 81.0%

: 122692-28-8
2-<3-phenylacetamido-4-thio(aminocarbonyl-methyl)-(3R,4R)-azetidin-2-on-1-yl>-trichloroethyl acetate

: 122692-59-5
2-<3-phenylacetamido-4-(aminocarbonyl-methyl)sulfonyl-(3R,4R)-azetidin-2-on-1-yl>-trichloroethyl acetate

Guidance literature:: With 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at 0 ℃; for 1h; then 20 deg C;
DOI:10.1016/0223-5234(88)90100-6