(2R,6S,8R,13aR)-3-Eth-(Z)-ylidene-13-methyl-1,3,4,7,8,13,13a,13b-octahydro-2H,6H-2,7-cyclo-6,8a-methano-pyrido[1',2':1,2]azepino[3,4-b]indol-8-ol

Base Information

Chemical Name:(2R,6S,8R,13aR)-3-Eth-(Z)-ylidene-13-methyl-1,3,4,7,8,13,13a,13b-octahydro-2H,6H-2,7-cyclo-6,8a-methano-pyrido[1',2':1,2]azepino[3,4-b]indol-8-ol
CAS No.:124016-72-4
Molecular Formula:C₂₀H₂₄N₂O
Molecular Weight:308.423
Hs Code.:

Synonyms:

Suppliers and Price of (2R,6S,8R,13aR)-3-Eth-(Z)-ylidene-13-methyl-1,3,4,7,8,13,13a,13b-octahydro-2H,6H-2,7-cyclo-6,8a-methano-pyrido[1',2':1,2]azepino[3,4-b]indol-8-ol

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,6S,8R,13aR)-3-Eth-(Z)-ylidene-13-methyl-1,3,4,7,8,13,13a,13b-octahydro-2H,6H-2,7-cyclo-6,8a-methano-pyrido[1',2':1,2]azepino[3,4-b]indol-8-ol

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (2R,6S,8R,13aR)-3-Eth-(Z)-ylidene-13-methyl-1,3,4,7,8,13,13a,13b-octahydro-2H,6H-2,7-cyclo-6,8a-methano-pyrido[1',2':1,2]azepino[3,4-b]indol-8-ol

There total 23 articles about (2R,6S,8R,13aR)-3-Eth-(Z)-ylidene-13-methyl-1,3,4,7,8,13,13a,13b-octahydro-2H,6H-2,7-cyclo-6,8a-methano-pyrido[1',2':1,2]azepino[3,4-b]indol-8-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: 95.0%

: 124016-71-3,137032-26-9
(2R,6S,8R,13aR)-3-Eth-(Z)-ylidene-8-(2-methoxy-ethoxymethoxy)-13-methyl-1,3,4,7,8,13,13a,13b-octahydro-2H,6H-2,7-cyclo-6,8a-methano-pyrido[1',2':1,2]azepino[3,4-b]indole

: 509-38-6,6883-73-4,124016-72-4
(2R,6S,8R,13aR)-3-Eth-(Z)-ylidene-13-methyl-1,3,4,7,8,13,13a,13b-octahydro-2H,6H-2,7-cyclo-6,8a-methano-pyrido[1',2':1,2]azepino[3,4-b]indol-8-ol

Guidance literature:: With hydrogenchloride; In methanol; for 5h; Heating;

Reference yield: 77.0%

: 124016-71-3,137032-26-9
(2R,6S,8R,13aR)-3-Eth-(E)-ylidene-8-(2-methoxy-ethoxymethoxy)-13-methyl-1,3,4,7,8,13,13a,13b-octahydro-2H,6H-2,7-cyclo-6,8a-methano-pyrido[1',2':1,2]azepino[3,4-b]indole

: 509-38-6,6883-73-4,124016-72-4
Tetraphyllicine

Guidance literature:: With hydrogenchloride; In methanol; for 5h; Heating;

Reference yield:

: 509-37-5,4360-12-7,6835-90-1,6989-79-3,22395-56-8,32999-94-3,51019-46-6,73089-81-3,149496-13-9
Ajmaline

: 509-38-6,6883-73-4,124016-72-4
Tetraphyllicine

Guidance literature:: Multi-step reaction with 10 steps

1: 1.) H₂SO₄, molecular sieves 3 Angstroem, 2.) NaOH / 1.) EtOH, 5 h, reflux, 2.) CH₂Cl₂, 0 deg C, 40 min

2: 75 percent / CuCl₂, phosphate buffer / tetrahydrofuran; H₂O / Ambient temperature

3: 81 percent / diisopropylamine / CH₂Cl₂ / 1.) 1.5 h, rt, 2.) 1.5 h, reflux

4: 71 percent / triethylamine / CH₂Cl₂ / 2.5 h / 0 °C

5: 76 percent / N-bromosuccinimide (NBS) / tetrahydrofuran / 0.5 h / -18 °C

6: 12 percent / 1,8-diazabicyclo<5,4,0>undec-7-ene (DBU) / dimethylformamide / 16 h / Ambient temperature

7: 65 percent / NaBH₄ / methanol / 0.5 h / Ambient temperature

8: 85 percent / NaOH / ethane-1,2-diol; H₂O / 6 h / Heating

9: 73 percent / mesyl chloride, pyridine / 0.5 h / Ambient temperature

10: 77 percent / conc. HCl / methanol / 5 h / Heating

With pyridine; hydrogenchloride; sodium hydroxide; sodium tetrahydroborate; N-Bromosuccinimide; phosphate buffer; 3 A molecular sieve; sulfuric acid; methanesulfonyl chloride; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; diisopropylamine; copper dichloride; In tetrahydrofuran; methanol; dichloromethane; water; ethylene glycol; N,N-dimethyl-formamide;