Methanesulfonic acid (R)-2-{(3S,3aS,6aR)-3-[2-(4-methoxy-benzyloxy)-ethyl]-hexahydro-cyclopenta[c]isoxazol-1-yl}-2-phenyl-ethyl ester

Base Information

Chemical Name:Methanesulfonic acid (R)-2-{(3S,3aS,6aR)-3-[2-(4-methoxy-benzyloxy)-ethyl]-hexahydro-cyclopenta[c]isoxazol-1-yl}-2-phenyl-ethyl ester
CAS No.:845276-49-5
Molecular Formula:C₂₅H₃₃NO₆S
Molecular Weight:475.606
Hs Code.:

Synonyms:Methanesulfonic acid (R)-2-{(3S,3aS,6aR)-3-[2-(4-methoxy-benzyloxy)-ethyl]-hexahydro-cyclopenta[c]isoxazol-1-yl}-2-phenyl-ethyl ester

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Chemical Property of Methanesulfonic acid (R)-2-{(3S,3aS,6aR)-3-[2-(4-methoxy-benzyloxy)-ethyl]-hexahydro-cyclopenta[c]isoxazol-1-yl}-2-phenyl-ethyl ester

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Technology Process of Methanesulfonic acid (R)-2-{(3S,3aS,6aR)-3-[2-(4-methoxy-benzyloxy)-ethyl]-hexahydro-cyclopenta[c]isoxazol-1-yl}-2-phenyl-ethyl ester

There total 5 articles about Methanesulfonic acid (R)-2-{(3S,3aS,6aR)-3-[2-(4-methoxy-benzyloxy)-ethyl]-hexahydro-cyclopenta[c]isoxazol-1-yl}-2-phenyl-ethyl ester 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: 98.0%

: 124-63-0
methanesulfonyl chloride

: 845276-48-4
(2R,3S,3aS,6aR)-2-{3-[2-(4-methoxyphenylmethyloxy)ethyl]hexahydrocyclopenta[c]isoxazol-1-yl}-2-phenyl-ethanol

: 845276-49-5
Methanesulfonic acid (R)-2-{(3S,3aS,6aR)-3-[2-(4-methoxy-benzyloxy)-ethyl]-hexahydro-cyclopenta[c]isoxazol-1-yl}-2-phenyl-ethyl ester

Guidance literature:: With triethylamine; In dichloromethane; at 0 ℃;
DOI:10.1055/s-2004-836049

Reference yield:

: 2746-25-0
p-Methoxybenzyl bromide

: 845276-49-5
Methanesulfonic acid (R)-2-{(3S,3aS,6aR)-3-[2-(4-methoxy-benzyloxy)-ethyl]-hexahydro-cyclopenta[c]isoxazol-1-yl}-2-phenyl-ethyl ester

Guidance literature:: Multi-step reaction with 7 steps

1.1: 91 percent / NaH / tetrahydrofuran; dimethylformamide

2.1: n-BuLi / tetrahydrofuran; hexamethylphosphoric acid triamide / -78 °C

2.2: tetrahydrofuran; hexamethylphosphoric acid triamide / -78 - 25 °C

3.1: H₂; pyridine / Pd/BaSO₄ / methanol / 25 °C / 760 Torr

4.1: toluene / 45 °C

5.1: toluene / 18 h / 75 °C

6.1: 84 percent / Zn(BH₄)2 / diethyl ether / -10 - 0 °C

7.1: 98 percent / Et₃N / CH₂Cl₂ / 0 °C

With pyridine; n-butyllithium; zinc(II) tetrahydroborate; hydrogen; sodium hydride; triethylamine; Pd-BaSO₄; In tetrahydrofuran; methanol; N,N,N,N,N,N-hexamethylphosphoric triamide; diethyl ether; dichloromethane; N,N-dimethyl-formamide; toluene;
DOI:10.1055/s-2004-836049

Reference yield:

: 218434-90-3
1-but-3-ynyloxymethyl-4-methoxy-benzene

: 845276-49-5
Methanesulfonic acid (R)-2-{(3S,3aS,6aR)-3-[2-(4-methoxy-benzyloxy)-ethyl]-hexahydro-cyclopenta[c]isoxazol-1-yl}-2-phenyl-ethyl ester

Guidance literature:: Multi-step reaction with 6 steps

1.1: n-BuLi / tetrahydrofuran; hexamethylphosphoric acid triamide / -78 °C

1.2: tetrahydrofuran; hexamethylphosphoric acid triamide / -78 - 25 °C

2.1: H₂; pyridine / Pd/BaSO₄ / methanol / 25 °C / 760 Torr

3.1: toluene / 45 °C

4.1: toluene / 18 h / 75 °C

5.1: 84 percent / Zn(BH₄)2 / diethyl ether / -10 - 0 °C

6.1: 98 percent / Et₃N / CH₂Cl₂ / 0 °C

With pyridine; n-butyllithium; zinc(II) tetrahydroborate; hydrogen; triethylamine; Pd-BaSO₄; In tetrahydrofuran; methanol; N,N,N,N,N,N-hexamethylphosphoric triamide; diethyl ether; dichloromethane; toluene;
DOI:10.1055/s-2004-836049