(R)-4-(2-Nitro-phenylselanyl)-2-(2S,12bS)-1,2,3,4,6,7,12,12b-octahydro-indolo[2,3-a]quinolizin-2-yl-butan-1-ol

Base Information

Chemical Name:(R)-4-(2-Nitro-phenylselanyl)-2-(2S,12bS)-1,2,3,4,6,7,12,12b-octahydro-indolo[2,3-a]quinolizin-2-yl-butan-1-ol
CAS No.:74447-18-0
Molecular Formula:C₂₅H₂₉N₃O₃Se
Molecular Weight:498.484
Hs Code.:

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Chemical Property of (R)-4-(2-Nitro-phenylselanyl)-2-(2S,12bS)-1,2,3,4,6,7,12,12b-octahydro-indolo[2,3-a]quinolizin-2-yl-butan-1-ol

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Technology Process of (R)-4-(2-Nitro-phenylselanyl)-2-(2S,12bS)-1,2,3,4,6,7,12,12b-octahydro-indolo[2,3-a]quinolizin-2-yl-butan-1-ol

There total 8 articles about (R)-4-(2-Nitro-phenylselanyl)-2-(2S,12bS)-1,2,3,4,6,7,12,12b-octahydro-indolo[2,3-a]quinolizin-2-yl-butan-1-ol 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: 39.2%

: 74447-17-9,137171-65-4,137172-75-9
(R)-(2S,12bS)-2-(1,2,3,4,6,7,12,12b-Octahydro-indolo[2,3-a]quinolizin-2-yl)-butane-1,4-diol

: 74447-18-0,137171-66-5
(R)-4-(2-Nitro-phenylselanyl)-2-(2S,12bS)-1,2,3,4,6,7,12,12b-octahydro-indolo[2,3-a]quinolizin-2-yl-butan-1-ol

Guidance literature:: With tributylphosphine; In tetrahydrofuran; for 2h; Ambient temperature;
DOI:10.1021/ja00532a061

Reference yield:

: 61-54-1
tryptamine

: 74447-18-0,137171-66-5
(R)-4-(2-Nitro-phenylselanyl)-2-(2S,12bS)-1,2,3,4,6,7,12,12b-octahydro-indolo[2,3-a]quinolizin-2-yl-butan-1-ol

Guidance literature:: Multi-step reaction with 4 steps

1: 1.) ethyl chloroformate, triethylamine / 1.) CH₂Cl₂, room temperature, 4 h, 2.) room temperature

2: 36.8 percent / methyl iodide / acetonitrile; H₂O / 48 h / Ambient temperature

3: 92.5 percent / LiAlH₄ / tetrahydrofuran / 3.5 h / Heating

4: 39.2 percent / tri-n-butylphosphine / tetrahydrofuran / 2 h / Ambient temperature

With lithium aluminium tetrahydride; tributylphosphine; chloroformic acid ethyl ester; triethylamine; methyl iodide; In tetrahydrofuran; water; acetonitrile;
DOI:10.1021/ja00532a061

Reference yield:

: 74447-10-2,80844-80-0
(S)-3-((1S,3R)-3-Hydroxy-cyclopentyl)-dihydro-furan-2-one

: 74447-18-0,137171-66-5
(R)-4-(2-Nitro-phenylselanyl)-2-(2S,12bS)-1,2,3,4,6,7,12,12b-octahydro-indolo[2,3-a]quinolizin-2-yl-butan-1-ol

Guidance literature:: Multi-step reaction with 7 steps

1: 79.8 percent / Jones Reagent

2: 2.) triethylamine

3: KOH / 2-methyl-propan-2-ol / 1 h / 60 °C

4: 1.) ethyl chloroformate, triethylamine / 1.) CH₂Cl₂, room temperature, 4 h, 2.) room temperature

5: 36.8 percent / methyl iodide / acetonitrile; H₂O / 48 h / Ambient temperature

6: 92.5 percent / LiAlH₄ / tetrahydrofuran / 3.5 h / Heating

7: 39.2 percent / tri-n-butylphosphine / tetrahydrofuran / 2 h / Ambient temperature

With potassium hydroxide; lithium aluminium tetrahydride; jones reagent; tributylphosphine; chloroformic acid ethyl ester; triethylamine; methyl iodide; In tetrahydrofuran; water; acetonitrile; tert-butyl alcohol;
DOI:10.1021/ja00532a061