(3R,4R)-3-azido-4-<(1S,2S)-1,2-<(isopropylidene)dioxy>-3-(methoxymethoxy)propanyl>-2-azetidinone

Base Information

Chemical Name:(3R,4R)-3-azido-4-<(1S,2S)-1,2-<(isopropylidene)dioxy>-3-(methoxymethoxy)propanyl>-2-azetidinone
CAS No.:130675-66-0
Molecular Formula:C₁₈H₂₄N₄O₅
Molecular Weight:376.412
Hs Code.:

Synonyms:(3R,4R)-3-azido-4-<(1S,2S)-1,2-<(isopropylidene)dioxy>-3-(methoxymethoxy)propanyl>-2-azetidinone

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Chemical Property of (3R,4R)-3-azido-4-<(1S,2S)-1,2-<(isopropylidene)dioxy>-3-(methoxymethoxy)propanyl>-2-azetidinone

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Technology Process of (3R,4R)-3-azido-4-<(1S,2S)-1,2-<(isopropylidene)dioxy>-3-(methoxymethoxy)propanyl>-2-azetidinone

There total 3 articles about (3R,4R)-3-azido-4-<(1S,2S)-1,2-<(isopropylidene)dioxy>-3-(methoxymethoxy)propanyl>-2-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:

Reference yield: 51.0%

: 50289-25-3
mixed anhydride of azidoacetic acid and trifluoroacetic anhydride

: 130675-65-9
Benzyl-[1-((4S,5S)-5-methoxymethoxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-meth-(E)-ylidene]-amine

: 130675-66-0
(3R,4R)-3-azido-4-<(1S,2S)-1,2-<(isopropylidene)dioxy>-3-(methoxymethoxy)propanyl>-2-azetidinone

Guidance literature:: With TEA; trifluoroacetic anhydride; In dichloromethane; at 0 ℃; for 12h;
DOI:10.1248/cpb.38.1601

Reference yield:

: 130675-64-8
(4R,5S)-5-Methoxymethoxymethyl-2,2-dimethyl-[1,3]dioxolane-4-carbaldehyde

: 130675-66-0
(3R,4R)-3-azido-4-<(1S,2S)-1,2-<(isopropylidene)dioxy>-3-(methoxymethoxy)propanyl>-2-azetidinone

Guidance literature:: Multi-step reaction with 2 steps

1: 100 percent / mollecular sieves 4 A / benzene / 2 h / Ambient temperature

2: 51 percent / TEA, trifluoroacetic anhydride / CH₂Cl₂ / 12 h / 0 °C

With 4 A molecular sieve; TEA; trifluoroacetic anhydride; In dichloromethane; benzene;
DOI:10.1248/cpb.38.1601

Reference yield:

: 100-46-9
benzylamine

: 130675-66-0
(3R,4R)-3-azido-4-<(1S,2S)-1,2-<(isopropylidene)dioxy>-3-(methoxymethoxy)propanyl>-2-azetidinone

Guidance literature:: Multi-step reaction with 2 steps

1: 100 percent / mollecular sieves 4 A / benzene / 2 h / Ambient temperature

2: 51 percent / TEA, trifluoroacetic anhydride / CH₂Cl₂ / 12 h / 0 °C

With 4 A molecular sieve; TEA; trifluoroacetic anhydride; In dichloromethane; benzene;
DOI:10.1248/cpb.38.1601