C₂₂H₂₉NO₆S

Base Information

Chemical Name:C₂₂H₂₉NO₆S
CAS No.:1616341-65-1
Molecular Formula:C₂₂H₂₉NO₆S
Molecular Weight:435.541
Hs Code.:

C<sub>22</sub>H<sub>29</sub>NO<sub>6</sub>S

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 C₂₂H₂₉NO₆S

Chemical Property:

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Technology Process of C₂₂H₂₉NO₆S

There total 4 articles about C₂₂H₂₉NO₆S 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:

: 134984-64-8
exo-2-aza-2-<(R)-1-phenylethyl>-3-ethoxycarbonyl<2.2.2>bicyclooct-5-ene

: 1616341-65-1
C₂₂H₂₉NO₆S

Guidance literature:: Multi-step reaction with 5 steps

1: N-iodo-succinimide; water / dimethyl sulfoxide / 3.5 h / 20 °C

2: 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride / toluene / 2 h / 100 °C

3: hydrogen; hydrogenchloride; 20% palladium hydroxide-activated charcoal / ethanol; 1,4-dioxane / 2 h

4: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 1 h / 20 °C

5: pyridine / tetrahydrofuran / 3 h / 0 - 20 °C

With pyridine; hydrogenchloride; N-iodo-succinimide; 2,2'-azobis(isobutyronitrile); 20% palladium hydroxide-activated charcoal; water; hydrogen; tri-n-butyl-tin hydride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; 1,4-dioxane; ethanol; dimethyl sulfoxide; toluene;

Reference yield:

: 851390-24-4
ethyl (1R,4R,5R,7S)-4-hydroxy-6-[(1R)-1-phenylethyl]-6-azabicyclo[3.2.1]octane-7-carboxylate

: 1616341-65-1
C₂₂H₂₉NO₆S

Guidance literature:: Multi-step reaction with 3 steps

1: hydrogen; hydrogenchloride; 20% palladium hydroxide-activated charcoal / ethanol; 1,4-dioxane / 2 h

2: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 1 h / 20 °C

3: pyridine / tetrahydrofuran / 3 h / 0 - 20 °C

With pyridine; hydrogenchloride; 20% palladium hydroxide-activated charcoal; hydrogen; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; 1,4-dioxane; ethanol;

Reference yield:

: C₁₈H₂₄INO₃

: 1616341-65-1
C₂₂H₂₉NO₆S

Guidance literature:: Multi-step reaction with 4 steps

1: 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride / toluene / 2 h / 100 °C

2: hydrogen; hydrogenchloride; 20% palladium hydroxide-activated charcoal / ethanol; 1,4-dioxane / 2 h

3: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 1 h / 20 °C

4: pyridine / tetrahydrofuran / 3 h / 0 - 20 °C

With pyridine; hydrogenchloride; 2,2'-azobis(isobutyronitrile); 20% palladium hydroxide-activated charcoal; hydrogen; tri-n-butyl-tin hydride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; 1,4-dioxane; ethanol; toluene;