(3RS,4SR)-1--4-ethynyl-3-phenoxyacetamidoazetidin-2-one

Base Information

Chemical Name:(3RS,4SR)-1--4-ethynyl-3-phenoxyacetamidoazetidin-2-one
CAS No.:99284-72-7
Molecular Formula:C₂₂H₂₀N₂O₆
Molecular Weight:408.411
Hs Code.:

(3RS,4SR)-1-<benzyloxycarbonyl(hydroxy)methyl>-4-ethynyl-3-phenoxyacetamidoazetidin-2-one

Synonyms:

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

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Chemical Property of (3RS,4SR)-1--4-ethynyl-3-phenoxyacetamidoazetidin-2-one

Chemical Property:

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Technology Process of (3RS,4SR)-1--4-ethynyl-3-phenoxyacetamidoazetidin-2-one

There total 1 articles about (3RS,4SR)-1--4-ethynyl-3-phenoxyacetamidoazetidin-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:

: 52709-42-9
benzylglyoxylate

: 85090-86-4,99284-71-6
(3RS,4SR)-4-ethynyl-3-phenoxyacetamidoazetidin-2-one

: 99284-72-7,99340-45-1
(3RS,4SR)-1--4-ethynyl-3-phenoxyacetamidoazetidin-2-one

Guidance literature:: With triethylamine; for 1h; Yield given; Ambient temperature;
DOI:10.1039/P19850001491

Reference yield:

: 99284-72-7,99340-45-1
(3RS,4SR)-1--4-ethynyl-3-phenoxyacetamidoazetidin-2-one

: 99300-03-5
Chloro-[(2R,3S)-2-ethynyl-4-oxo-3-(2-phenoxy-acetylamino)-azetidin-1-yl]-acetic acid benzyl ester

Guidance literature:: With 2,6-dimethylpyridine; thionyl chloride; In tetrahydrofuran; at -15 ℃;
DOI:10.1039/P19850001491

Reference yield:

: 99284-72-7,99340-45-1
(3RS,4SR)-1--4-ethynyl-3-phenoxyacetamidoazetidin-2-one

: 85090-85-3
(3bRS,4RS,7SR) 4,5-dihydro-5-oxo-4-phenoxyacetamido-3bH-azeto<1',2':3,4>imidazo<1,5-c>-v-triazole-7-carboxylic acid

Guidance literature:: Multi-step reaction with 4 steps

1: 400 mg / 2,6-dimethylpyridine, thionylchloride / tetrahydrofuran / -15 °C

2: 76 percent / sodium azide / dimethylformamide / 0.08 h

3: 18 percent / toluene / 36 h / Heating

4: 72 percent / hydrogen / 10percent Pd-C / dioxane; H₂O / 0.75 h

With 2,6-dimethylpyridine; thionyl chloride; sodium azide; hydrogen; palladium on activated charcoal; In tetrahydrofuran; 1,4-dioxane; water; N,N-dimethyl-formamide; toluene;
DOI:10.1039/P19850001491