((1R,5S,8R)-8-Hydroxy-4,4,8-trimethyl-3-aza-bicyclo[3.3.1]non-2-en-2-yl)-[1-(4-methoxy-benzenesulfonyl)-1H-indol-3-yl]-methanone

Base Information

Chemical Name:((1R,5S,8R)-8-Hydroxy-4,4,8-trimethyl-3-aza-bicyclo[3.3.1]non-2-en-2-yl)-[1-(4-methoxy-benzenesulfonyl)-1H-indol-3-yl]-methanone
CAS No.:1025893-85-9
Molecular Formula:C₂₇H₃₀N₂O₅S
Molecular Weight:494.612
Hs Code.:

Synonyms:((1R,5S,8R)-8-Hydroxy-4,4,8-trimethyl-3-aza-bicyclo[3.3.1]non-2-en-2-yl)-[1-(4-methoxy-benzenesulfonyl)-1H-indol-3-yl]-methanone

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Chemical Property of ((1R,5S,8R)-8-Hydroxy-4,4,8-trimethyl-3-aza-bicyclo[3.3.1]non-2-en-2-yl)-[1-(4-methoxy-benzenesulfonyl)-1H-indol-3-yl]-methanone

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Technology Process of ((1R,5S,8R)-8-Hydroxy-4,4,8-trimethyl-3-aza-bicyclo[3.3.1]non-2-en-2-yl)-[1-(4-methoxy-benzenesulfonyl)-1H-indol-3-yl]-methanone

There total 6 articles about ((1R,5S,8R)-8-Hydroxy-4,4,8-trimethyl-3-aza-bicyclo[3.3.1]non-2-en-2-yl)-[1-(4-methoxy-benzenesulfonyl)-1H-indol-3-yl]-methanone 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: 56.0%

: 159979-28-9
(1S,4R,5R,6R)-4-[1-(4-Methoxy-benzenesulfonyl)-1H-indol-3-ylmethyl]-2,2,6-trimethyl-3-aza-bicyclo[3.3.1]nonan-6-ol

: 1025893-85-9
((1R,5S,8R)-8-Hydroxy-4,4,8-trimethyl-3-aza-bicyclo[3.3.1]non-2-en-2-yl)-[1-(4-methoxy-benzenesulfonyl)-1H-indol-3-yl]-methanone

Guidance literature:: With osmium(VIII) oxide; 4-methylmorpholine N-oxide; In 1,4-dioxane; water; at 25 ℃; for 72h;
DOI:10.1016/S0957-4166(00)86278-3

Reference yield:

: 18172-67-3,19902-08-0,25719-60-2
beta-pinene

: 1025893-85-9
((1R,5S,8R)-8-Hydroxy-4,4,8-trimethyl-3-aza-bicyclo[3.3.1]non-2-en-2-yl)-[1-(4-methoxy-benzenesulfonyl)-1H-indol-3-yl]-methanone

Guidance literature:: Multi-step reaction with 6 steps

1: 1.) Hg(NO₃)2, 2.) 1N aq. NaOH, NaBH₄, 3.) 18percent aq. HCl

2: 1.) NaH / 1.) THF, 0 deg C, 2 h, 2.) THF, 25 deg C, 16 h

3: 3 percent / N-methylmorpholine N-oxide, OsO₄ / dioxane; H₂O / 48 h / 25 °C

4: 89 percent / aq. NaIO₄ / tetrahydrofuran / 12 h / 25 °C

5: 91 percent / diethyl ether / -78 °C

6: 56 percent / N-methylmorpholine N-oxide, OsO₄ / dioxane; H₂O / 72 h / 25 °C

With hydrogenchloride; sodium hydroxide; sodium tetrahydroborate; sodium periodate; osmium(VIII) oxide; sodium hydride; mercury(II) nitrate; 4-methylmorpholine N-oxide; In tetrahydrofuran; 1,4-dioxane; diethyl ether; water;
DOI:10.1016/S0957-4166(00)86278-3

Reference yield:

: 79559-56-1
(+)-makomakine

: 1025893-85-9
((1R,5S,8R)-8-Hydroxy-4,4,8-trimethyl-3-aza-bicyclo[3.3.1]non-2-en-2-yl)-[1-(4-methoxy-benzenesulfonyl)-1H-indol-3-yl]-methanone

Guidance literature:: Multi-step reaction with 5 steps

1: 1.) NaH / 1.) THF, 0 deg C, 2 h, 2.) THF, 25 deg C, 16 h

2: 3 percent / N-methylmorpholine N-oxide, OsO₄ / dioxane; H₂O / 48 h / 25 °C

3: 89 percent / aq. NaIO₄ / tetrahydrofuran / 12 h / 25 °C

4: 91 percent / diethyl ether / -78 °C

5: 56 percent / N-methylmorpholine N-oxide, OsO₄ / dioxane; H₂O / 72 h / 25 °C

With sodium periodate; osmium(VIII) oxide; sodium hydride; 4-methylmorpholine N-oxide; In tetrahydrofuran; 1,4-dioxane; diethyl ether; water;
DOI:10.1016/S0957-4166(00)86278-3