(1S,4R,6S)-6-(1-Benzenesulfonyl-1H-indol-2-yl)-2-ethyl-8,8-dimethoxy-2-aza-bicyclo[2.2.2]octane-6-carboxylic acid methyl ester

Base Information

Chemical Name:(1S,4R,6S)-6-(1-Benzenesulfonyl-1H-indol-2-yl)-2-ethyl-8,8-dimethoxy-2-aza-bicyclo[2.2.2]octane-6-carboxylic acid methyl ester
CAS No.:108713-35-5
Molecular Formula:C₂₇H₃₂N₂O₆S
Molecular Weight:512.627
Hs Code.:

Synonyms:(1S,4R,6S)-6-(1-Benzenesulfonyl-1H-indol-2-yl)-2-ethyl-8,8-dimethoxy-2-aza-bicyclo[2.2.2]octane-6-carboxylic acid methyl ester

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Chemical Property of (1S,4R,6S)-6-(1-Benzenesulfonyl-1H-indol-2-yl)-2-ethyl-8,8-dimethoxy-2-aza-bicyclo[2.2.2]octane-6-carboxylic acid methyl ester

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Technology Process of (1S,4R,6S)-6-(1-Benzenesulfonyl-1H-indol-2-yl)-2-ethyl-8,8-dimethoxy-2-aza-bicyclo[2.2.2]octane-6-carboxylic acid methyl ester

There total 4 articles about (1S,4R,6S)-6-(1-Benzenesulfonyl-1H-indol-2-yl)-2-ethyl-8,8-dimethoxy-2-aza-bicyclo[2.2.2]octane-6-carboxylic acid methyl 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: 76.0%

: 108713-19-5
methyl 8,8-dimethoxy-6-exo-<1-(phenylsulfonyl)indol-2-yl>-8-methoxy-2-azabicyclo<2.2.2>octane-6-endo-carboxylate

: 75-03-6
ethyl iodide

: 108713-35-5
(1S,4R,6S)-6-(1-Benzenesulfonyl-1H-indol-2-yl)-2-ethyl-8,8-dimethoxy-2-aza-bicyclo[2.2.2]octane-6-carboxylic acid methyl ester

Guidance literature:: With potassium carbonate; In acetonitrile; for 3h;
DOI:10.1021/jo00390a034

Reference yield:

: 620-08-6,1232006-56-2
4-methoxypyridine

: 108713-35-5
(1S,4R,6S)-6-(1-Benzenesulfonyl-1H-indol-2-yl)-2-ethyl-8,8-dimethoxy-2-aza-bicyclo[2.2.2]octane-6-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 1.) sodium borohydride / 1.) methanol, -78 deg C, 15 min, 2.) methanol, -78 deg C, 15 min

2: 55 percent / xylene / 72 h / 68 - 70 °C

3: 90 percent / cyclohexadiene, trifluoroacetic acid / 10percent Pd/C / 1 h / 25 °C

4: 76 percent / potassium carbonate / acetonitrile / 3 h

With sodium tetrahydroborate; potassium carbonate; cyclohexa-1,3-diene; trifluoroacetic acid; palladium on activated charcoal; In acetonitrile; xylene;
DOI:10.1021/jo00390a034

Reference yield:

: 108713-16-2
methyl 2-<(benzyloxy)carbonyl>-6-exo-<1-(phenylsulfonyl)indol-2-yl>-8-methoxy-2-azabicyclo<2.2.2>oct-7-ene-6-endo-carboxylate

: 108713-35-5
(1S,4R,6S)-6-(1-Benzenesulfonyl-1H-indol-2-yl)-2-ethyl-8,8-dimethoxy-2-aza-bicyclo[2.2.2]octane-6-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 90 percent / cyclohexadiene, trifluoroacetic acid / 10percent Pd/C / 1 h / 25 °C

2: 76 percent / potassium carbonate / acetonitrile / 3 h

With potassium carbonate; cyclohexa-1,3-diene; trifluoroacetic acid; palladium on activated charcoal; In acetonitrile;
DOI:10.1021/jo00390a034