(3aR,4R,7R,7aR)-4-allyl-1-[(2-nitrophenyl)sulfonyl]-7-(pent-4-en-1-yl)hexahydro-1H-indol-5(6H)-one?

Base Information

Chemical Name:(3aR,4R,7R,7aR)-4-allyl-1-[(2-nitrophenyl)sulfonyl]-7-(pent-4-en-1-yl)hexahydro-1H-indol-5(6H)-one?
CAS No.:1429924-75-3
Molecular Formula:C₂₂H₂₈N₂O₅S
Molecular Weight:432.541
Hs Code.:

Synonyms:(3aR,4R,7R,7aR)-4-allyl-1-[(2-nitrophenyl)sulfonyl]-7-(pent-4-en-1-yl)hexahydro-1H-indol-5(6H)-one?

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Chemical Property of (3aR,4R,7R,7aR)-4-allyl-1-[(2-nitrophenyl)sulfonyl]-7-(pent-4-en-1-yl)hexahydro-1H-indol-5(6H)-one?

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Technology Process of (3aR,4R,7R,7aR)-4-allyl-1-[(2-nitrophenyl)sulfonyl]-7-(pent-4-en-1-yl)hexahydro-1H-indol-5(6H)-one?

There total 7 articles about (3aR,4R,7R,7aR)-4-allyl-1-[(2-nitrophenyl)sulfonyl]-7-(pent-4-en-1-yl)hexahydro-1H-indol-5(6H)-one? 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: 55.0%

: 1429924-74-2
N-{2-[(1R,2R,5R,6S)-2-allyl-6-hydroxy-3-oxo-5-(pent-4-en-1-yl)cyclohexyl]ethyl}-2-nitrobenzenesulfonamide

: 1429924-75-3
(3aR,4R,7R,7aR)-4-allyl-1-[(2-nitrophenyl)sulfonyl]-7-(pent-4-en-1-yl)hexahydro-1H-indol-5(6H)-one?

Guidance literature:: With di-isopropyl azodicarboxylate; triphenylphosphine; In 1,4-dioxane; toluene; at 20 ℃; for 0.25h; Inert atmosphere;
DOI:10.1002/chem.201200376

Reference yield:

: 1429924-72-0
2-{(1R,2R,5R,6S)-2-allyl-6-[(1R,2R)-2-hydroxy-1,2-diphenylethoxy]-3-oxo-5-(pent-4-en-1-yl)cyclohexyl}acetaldehyde

: 1429924-75-3
(3aR,4R,7R,7aR)-4-allyl-1-[(2-nitrophenyl)sulfonyl]-7-(pent-4-en-1-yl)hexahydro-1H-indol-5(6H)-one?

Guidance literature:: Multi-step reaction with 4 steps

1: sodium tris(acetoxy)borohydride / 1,2-dichloro-ethane / 1.5 h / 0 - 20 °C / Inert atmosphere

2: triethylamine / dichloromethane / 0.5 h / 0 - 20 °C / Inert atmosphere

3: ammonium cerium (IV) nitrate / acetonitrile; water / 5 h / 20 °C

4: di-isopropyl azodicarboxylate; triphenylphosphine / toluene; 1,4-dioxane / 0.25 h / 20 °C / Inert atmosphere

With ammonium cerium (IV) nitrate; di-isopropyl azodicarboxylate; sodium tris(acetoxy)borohydride; triethylamine; triphenylphosphine; In 1,4-dioxane; dichloromethane; water; 1,2-dichloro-ethane; toluene; acetonitrile;
DOI:10.1002/chem.201200376

Reference yield:

: 1429924-73-1
N-(2-{(1R,2R,5R,6S)-2-allyl-6-[(1R,2R)-2-hydroxy-1,2-diphenylethoxy]-3-oxo-5-(pent-4-en-1-yl)cyclohexyl}ethyl)-N-(4-methoxybenzyl)-2-nitrobenzenesulfonamide

: 1429924-75-3
(3aR,4R,7R,7aR)-4-allyl-1-[(2-nitrophenyl)sulfonyl]-7-(pent-4-en-1-yl)hexahydro-1H-indol-5(6H)-one?

Guidance literature:: Multi-step reaction with 2 steps

1: ammonium cerium (IV) nitrate / acetonitrile; water / 5 h / 20 °C

2: di-isopropyl azodicarboxylate; triphenylphosphine / toluene; 1,4-dioxane / 0.25 h / 20 °C / Inert atmosphere

With ammonium cerium (IV) nitrate; di-isopropyl azodicarboxylate; triphenylphosphine; In 1,4-dioxane; water; toluene; acetonitrile;
DOI:10.1002/chem.201200376