(αξ)-α-<(1ξ)-<(ξ)-2-methylenecyclopentyl>ethyl>-1-(phenylsulfonyl)-α-<(phenylsulfonyl)methyl>-1H-pyrrole-3-methanol

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Chemical Name:(αξ)-α-<(1ξ)-<(ξ)-2-methylenecyclopentyl>ethyl>-1-(phenylsulfonyl)-α-<(phenylsulfonyl)methyl>-1H-pyrrole-3-methanol
CAS No.:157331-45-8
Molecular Formula:C₂₆H₂₉NO₅S₂
Molecular Weight:499.652
Hs Code.:

Synonyms:(αξ)-α-<(1ξ)-<(ξ)-2-methylenecyclopentyl>ethyl>-1-(phenylsulfonyl)-α-<(phenylsulfonyl)methyl>-1H-pyrrole-3-methanol

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Chemical Property of (αξ)-α-<(1ξ)-<(ξ)-2-methylenecyclopentyl>ethyl>-1-(phenylsulfonyl)-α-<(phenylsulfonyl)methyl>-1H-pyrrole-3-methanol

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Technology Process of (αξ)-α-<(1ξ)-<(ξ)-2-methylenecyclopentyl>ethyl>-1-(phenylsulfonyl)-α-<(phenylsulfonyl)methyl>-1H-pyrrole-3-methanol

There total 5 articles about (αξ)-α-<(1ξ)-<(ξ)-2-methylenecyclopentyl>ethyl>-1-(phenylsulfonyl)-α-<(phenylsulfonyl)methyl>-1H-pyrrole-3-methanol 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:

: 88075-95-0
1-(phenylsulfonyl)-1H-pyrrole-3-carbaldehyde

: 157331-45-8
(αξ)-α-<(1ξ)-<(ξ)-2-methylenecyclopentyl>ethyl>-1-(phenylsulfonyl)-α-<(phenylsulfonyl)methyl>-1H-pyrrole-3-methanol

Guidance literature:: Multi-step reaction with 4 steps

1: 1.) lithium diisopropylamide / 1.) THF, -82 deg C to -69 deg C, 45 min, 2.) THF, -69 deg C to -59 deg C, 1 h

2: 84 percent / MnO₂ / CH₂Cl₂ / 2 h / Heating

3: 70 percent / LiCl, H₂O / hexamethylphosphoric acid triamide / 14 h / 130 - 135 °C

4: 1.) n-BuLi / 1.) THF, hexane a) -80 deg C to -72 deg C, 20 min, b) -20 deg C, 10 min, 2.) THF, hexane, -80 deg C to -75 deg C, 20 min

With manganese(IV) oxide; n-butyllithium; water; lithium chloride; lithium diisopropyl amide; In N,N,N,N,N,N-hexamethylphosphoric triamide; dichloromethane;
DOI:10.1248/cpb.42.846

Reference yield:

: 157331-37-8
ethyl α-methyl-2-methylene-1-cyclopentaneacetate

: 157331-45-8
(αξ)-α-<(1ξ)-<(ξ)-2-methylenecyclopentyl>ethyl>-1-(phenylsulfonyl)-α-<(phenylsulfonyl)methyl>-1H-pyrrole-3-methanol

Guidance literature:: Multi-step reaction with 4 steps

1: 1.) lithium diisopropylamide / 1.) THF, -82 deg C to -69 deg C, 45 min, 2.) THF, -69 deg C to -59 deg C, 1 h

2: 84 percent / MnO₂ / CH₂Cl₂ / 2 h / Heating

3: 70 percent / LiCl, H₂O / hexamethylphosphoric acid triamide / 14 h / 130 - 135 °C

4: 1.) n-BuLi / 1.) THF, hexane a) -80 deg C to -72 deg C, 20 min, b) -20 deg C, 10 min, 2.) THF, hexane, -80 deg C to -75 deg C, 20 min

With manganese(IV) oxide; n-butyllithium; water; lithium chloride; lithium diisopropyl amide; In N,N,N,N,N,N-hexamethylphosphoric triamide; dichloromethane;
DOI:10.1248/cpb.42.846

Reference yield:

: 157331-40-3
ethyl (αξ)-α-methyl-α-<(ξ)-2-methylenecyclopentyl>-β-oxo-1-(phenylsulfonyl)-1H-pyrrole-3-propanoate

: 157331-45-8
(αξ)-α-<(1ξ)-<(ξ)-2-methylenecyclopentyl>ethyl>-1-(phenylsulfonyl)-α-<(phenylsulfonyl)methyl>-1H-pyrrole-3-methanol

Guidance literature:: Multi-step reaction with 2 steps

1: 70 percent / LiCl, H₂O / hexamethylphosphoric acid triamide / 14 h / 130 - 135 °C

2: 1.) n-BuLi / 1.) THF, hexane a) -80 deg C to -72 deg C, 20 min, b) -20 deg C, 10 min, 2.) THF, hexane, -80 deg C to -75 deg C, 20 min

With n-butyllithium; water; lithium chloride; In N,N,N,N,N,N-hexamethylphosphoric triamide;
DOI:10.1248/cpb.42.846