(2R,6R)-6-(allyloxymethyl)-12-benzyl-2-vinyl-1,2,3,6,7,12b-hexahydroindolo[2,3-a]quinolizin-4(12H)-one

Base Information

Chemical Name:(2R,6R)-6-(allyloxymethyl)-12-benzyl-2-vinyl-1,2,3,6,7,12b-hexahydroindolo[2,3-a]quinolizin-4(12H)-one
CAS No.:1360734-98-0
Molecular Formula:C₂₈H₃₀N₂O₂
Molecular Weight:426.558
Hs Code.:

Synonyms:(2R,6R)-6-(allyloxymethyl)-12-benzyl-2-vinyl-1,2,3,6,7,12b-hexahydroindolo[2,3-a]quinolizin-4(12H)-one

Suppliers and Price of (2R,6R)-6-(allyloxymethyl)-12-benzyl-2-vinyl-1,2,3,6,7,12b-hexahydroindolo[2,3-a]quinolizin-4(12H)-one

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of (2R,6R)-6-(allyloxymethyl)-12-benzyl-2-vinyl-1,2,3,6,7,12b-hexahydroindolo[2,3-a]quinolizin-4(12H)-one

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (2R,6R)-6-(allyloxymethyl)-12-benzyl-2-vinyl-1,2,3,6,7,12b-hexahydroindolo[2,3-a]quinolizin-4(12H)-one

There total 6 articles about (2R,6R)-6-(allyloxymethyl)-12-benzyl-2-vinyl-1,2,3,6,7,12b-hexahydroindolo[2,3-a]quinolizin-4(12H)-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: 37.0%

: 1360734-99-1
(6R)-6-(allyloxymethyl)-12-benzyl-1,6,7,12b-tetrahydroindolo[2,3-a]quinolizin-4(12H)-one

: 1826-67-1
vinyl magnesium bromide

: 1360734-98-0
(2R,6R)-6-(allyloxymethyl)-12-benzyl-2-vinyl-1,2,3,6,7,12b-hexahydroindolo[2,3-a]quinolizin-4(12H)-one

Guidance literature:: vinyl magnesium bromide; With copper(I) cyanide; In tetrahydrofuran; at -78 - 0 ℃;

(6R)-6-(allyloxymethyl)-12-benzyl-1,6,7,12b-tetrahydroindolo[2,3-a]quinolizin-4(12H)-one; In tetrahydrofuran; at -78 ℃; for 0.0833333h;

With chloro-trimethyl-silane; In tetrahydrofuran; at -78 - 20 ℃;
DOI:10.1016/j.bmcl.2011.12.071

Reference yield:

: 1360734-87-7
(6R,12bS)-12-benzyl-6-(hydroxymethyl)-1,2,3,6,7,12b-hexahydroindolo[2,3-a]quinolizin-4(12H)-one

: 1360734-98-0
(2R,6R)-6-(allyloxymethyl)-12-benzyl-2-vinyl-1,2,3,6,7,12b-hexahydroindolo[2,3-a]quinolizin-4(12H)-one

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium hydride / N,N-dimethyl-formamide / 0.5 h / 0 - 20 °C / Inert atmosphere

1.2: 24 h / Inert atmosphere

2.1: n-butyllithium; N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 1 h / -78 °C / Inert atmosphere

2.2: 24 h / Inert atmosphere

3.1: sodium periodate; sodium hydrogencarbonate / methanol; water / 24 h / 60 °C

4.1: copper(I) cyanide / tetrahydrofuran / -78 - 0 °C

4.2: 0.08 h / -78 °C

4.3: -78 - 20 °C

With sodium periodate; n-butyllithium; copper(I) cyanide; sodium hydride; sodium hydrogencarbonate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; methanol; water; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2011.12.071

Reference yield:

: 1360734-90-2
(6R)-6-(allyloxymethyl)-12-benzyl-1,2,3,6,7,12b-hexahydroindolo[2,3-a]quinolizin-4(12H)-one

: 1360734-98-0
(2R,6R)-6-(allyloxymethyl)-12-benzyl-2-vinyl-1,2,3,6,7,12b-hexahydroindolo[2,3-a]quinolizin-4(12H)-one

Guidance literature:: Multi-step reaction with 3 steps

1.1: n-butyllithium; N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 1 h / -78 °C / Inert atmosphere

1.2: 24 h / Inert atmosphere

2.1: sodium periodate; sodium hydrogencarbonate / methanol; water / 24 h / 60 °C

3.1: copper(I) cyanide / tetrahydrofuran / -78 - 0 °C

3.2: 0.08 h / -78 °C

3.3: -78 - 20 °C

With sodium periodate; n-butyllithium; copper(I) cyanide; sodium hydrogencarbonate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; methanol; water;
DOI:10.1016/j.bmcl.2011.12.071