tert-butyl (1R,2S,5S)-7-(N-benzyl-4-methylphenylsulfonamido)-6-cyclohexyl-2-hydroxybicyclo[3.2.0]hept-6-ene-1-carboxylate

Base Information

Chemical Name:tert-butyl (1R,2S,5S)-7-(N-benzyl-4-methylphenylsulfonamido)-6-cyclohexyl-2-hydroxybicyclo[3.2.0]hept-6-ene-1-carboxylate
CAS No.:1290632-01-7
Molecular Formula:C₃₂H₄₁NO₅S
Molecular Weight:551.747
Hs Code.:

Synonyms:tert-butyl (1R,2S,5S)-7-(N-benzyl-4-methylphenylsulfonamido)-6-cyclohexyl-2-hydroxybicyclo[3.2.0]hept-6-ene-1-carboxylate

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Chemical Property of tert-butyl (1R,2S,5S)-7-(N-benzyl-4-methylphenylsulfonamido)-6-cyclohexyl-2-hydroxybicyclo[3.2.0]hept-6-ene-1-carboxylate

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Technology Process of tert-butyl (1R,2S,5S)-7-(N-benzyl-4-methylphenylsulfonamido)-6-cyclohexyl-2-hydroxybicyclo[3.2.0]hept-6-ene-1-carboxylate

There total 3 articles about tert-butyl (1R,2S,5S)-7-(N-benzyl-4-methylphenylsulfonamido)-6-cyclohexyl-2-hydroxybicyclo[3.2.0]hept-6-ene-1-carboxylate 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: 94.0%

: 1290631-83-2
(1R,5S)-tert-butyl-7-[N-benzyl-4-methylphenylsulfonamido]-6-cyclohexyl-2-oxobicyclo[3.2.0]hept-6-ene-1-carboxylate

: 1290632-01-7
tert-butyl (1R,2S,5S)-7-(N-benzyl-4-methylphenylsulfonamido)-6-cyclohexyl-2-hydroxybicyclo[3.2.0]hept-6-ene-1-carboxylate

Guidance literature:: With sodium tetrahydroborate; In methanol; dichloromethane; at 0 ℃; for 0.5h; diastereoselective reaction; Inert atmosphere;
DOI:10.1055/s-0031-1289679

Reference yield:

: 1116153-61-7
N-benzyl-N-(cyclohexylethynyl)-4-methylbenzenesulfonamide

: 1290632-01-7
tert-butyl (1R,2S,5S)-7-(N-benzyl-4-methylphenylsulfonamido)-6-cyclohexyl-2-hydroxybicyclo[3.2.0]hept-6-ene-1-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1.1: RuCl2(κ4-N,N'-bis[o-(diphenylphosphino)benzylidene]-(1S,2S)-diiminocyclohexane); triethyloxonium hexaflourophosphate / dichloromethane / 0.17 h / 20 °C / Inert atmosphere

1.2: 24 h / 55 °C / Inert atmosphere

2.1: sodium tetrahydroborate / methanol; dichloromethane / 0.5 h / 0 °C / Inert atmosphere

With sodium tetrahydroborate; RuCl2(κ4-N,N'-bis[o-(diphenylphosphino)benzylidene]-(1S,2S)-diiminocyclohexane); triethyloxonium hexaflourophosphate; In methanol; dichloromethane; 1.1: Ficini reaction / 1.2: Ficini reaction;
DOI:10.1055/s-0031-1289679

Reference yield:

: tert‐butyl 5‐oxocyclopent‐1‐ene‐1‐carboxylate

: 1290632-01-7
tert-butyl (1R,2S,5S)-7-(N-benzyl-4-methylphenylsulfonamido)-6-cyclohexyl-2-hydroxybicyclo[3.2.0]hept-6-ene-1-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1.1: RuCl2(κ4-N,N'-bis[o-(diphenylphosphino)benzylidene]-(1S,2S)-diiminocyclohexane); triethyloxonium hexaflourophosphate / dichloromethane / 0.17 h / 20 °C / Inert atmosphere

1.2: 24 h / 55 °C / Inert atmosphere

2.1: sodium tetrahydroborate / methanol; dichloromethane / 0.5 h / 0 °C / Inert atmosphere

With sodium tetrahydroborate; RuCl2(κ4-N,N'-bis[o-(diphenylphosphino)benzylidene]-(1S,2S)-diiminocyclohexane); triethyloxonium hexaflourophosphate; In methanol; dichloromethane; 1.1: Ficini reaction / 1.2: Ficini reaction;
DOI:10.1055/s-0031-1289679