(3S,4S)-4-<(S)-1-((4-benzyloxycarbonylpiperazin-1-yl)carbonyloxy)ethyl>-3-<(R)-1-tetrahydropyran-2-yloxyethyl>-2-azetidinone

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Chemical Name:(3S,4S)-4-<(S)-1-((4-benzyloxycarbonylpiperazin-1-yl)carbonyloxy)ethyl>-3-<(R)-1-tetrahydropyran-2-yloxyethyl>-2-azetidinone
CAS No.:130163-63-2
Molecular Formula:C₂₅H₃₅N₃O₇
Molecular Weight:489.569
Hs Code.:

Synonyms:(3S,4S)-4-<(S)-1-((4-benzyloxycarbonylpiperazin-1-yl)carbonyloxy)ethyl>-3-<(R)-1-tetrahydropyran-2-yloxyethyl>-2-azetidinone

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Chemical Property of (3S,4S)-4-<(S)-1-((4-benzyloxycarbonylpiperazin-1-yl)carbonyloxy)ethyl>-3-<(R)-1-tetrahydropyran-2-yloxyethyl>-2-azetidinone

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Technology Process of (3S,4S)-4-<(S)-1-((4-benzyloxycarbonylpiperazin-1-yl)carbonyloxy)ethyl>-3-<(R)-1-tetrahydropyran-2-yloxyethyl>-2-azetidinone

There total 5 articles about (3S,4S)-4-<(S)-1-((4-benzyloxycarbonylpiperazin-1-yl)carbonyloxy)ethyl>-3-<(R)-1-tetrahydropyran-2-yloxyethyl>-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: 91.0%

: 31166-44-6
phenylmethyl 1-piperazinecarboxylate

: 130163-58-5
(3S,4S)-3-<(R)-1-tetrahydropyran-2-yloxyethyl>-4-<(S)-1-(p-nitrophenoxycarbonyloxy)ethyl>-2-azetidinone

: 130163-63-2
(3S,4S)-4-<(S)-1-((4-benzyloxycarbonylpiperazin-1-yl)carbonyloxy)ethyl>-3-<(R)-1-tetrahydropyran-2-yloxyethyl>-2-azetidinone

Guidance literature:: In methanol; at 0 ℃; for 1h;
DOI:10.1248/cpb.38.917

Reference yield:

: 110-87-2
3,4-dihydro-2H-pyran

: 130163-63-2
(3S,4S)-4-<(S)-1-((4-benzyloxycarbonylpiperazin-1-yl)carbonyloxy)ethyl>-3-<(R)-1-tetrahydropyran-2-yloxyethyl>-2-azetidinone

Guidance literature:: Multi-step reaction with 4 steps

1: 98 percent / pyridinium p-toluenesulfonate / CH₂Cl₂ / 2 h / Ambient temperature

2: 100 percent / 1N HCl, hydrogen / 5percent Pd-C / tetrahydrofuran / 5.5 h / Ambient temperature

3: 97 percent / pyridine / 17 h / Ambient temperature

4: 91 percent / methanol / 1 h / 0 °C

With pyridine; hydrogenchloride; hydrogen; pyridinium p-toluenesulfonate; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1248/cpb.38.917

Reference yield:

: 112256-71-0
(3S,4S)-4-<(S)-1-benzyloxyethyl>-3-<(R)-1-hydroxyethyl>-2-azetidinone

: 130163-63-2
(3S,4S)-4-<(S)-1-((4-benzyloxycarbonylpiperazin-1-yl)carbonyloxy)ethyl>-3-<(R)-1-tetrahydropyran-2-yloxyethyl>-2-azetidinone

Guidance literature:: Multi-step reaction with 4 steps

1: 98 percent / pyridinium p-toluenesulfonate / CH₂Cl₂ / 2 h / Ambient temperature

2: 100 percent / 1N HCl, hydrogen / 5percent Pd-C / tetrahydrofuran / 5.5 h / Ambient temperature

3: 97 percent / pyridine / 17 h / Ambient temperature

4: 91 percent / methanol / 1 h / 0 °C

With pyridine; hydrogenchloride; hydrogen; pyridinium p-toluenesulfonate; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1248/cpb.38.917