(+/-)-Tortuosamine

Base Information

Chemical Name:(+/-)-Tortuosamine
CAS No.:79517-20-7
Molecular Formula:C₂₀H₂₆N₂O₂
Molecular Weight:326.439
Hs Code.:
UNII:XH338JMK8P
DSSTox Substance ID:DTXSID501045656
Wikidata:Q105219728

Synonyms:(+/-)-Tortuosamine;Tortuosamine, (+/-)-;XH338JMK8P;UNII-XH338JMK8P;79517-20-7;6-(3,4-Dimethoxyphenyl)-5,6,7,8-tetrahydro-N-methyl-6-quinolineethanamine;6-Quinolineethanamine, 6-(3,4-dimethoxyphenyl)-5,6,7,8-tetrahydro-N-methyl-;6-Quinolineethanamine, 6-(3,4-dimethoxyphenyl)-5,6,7,8-tetrahydro-N-methyl-, (+/-)-;(+-)-Tortuosamine;DTXSID501045656

Suppliers and Price of (+/-)-Tortuosamine

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
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Total 0 raw suppliers

Chemical Property of (+/-)-Tortuosamine

Chemical Property:

XLogP3:3.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:6
Exact Mass:326.199428076
Heavy Atom Count:24
Complexity:392

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CNCCC1(CCC2=C(C1)C=CC=N2)C3=CC(=C(C=C3)OC)OC

Technology Process of (+/-)-Tortuosamine

There total 17 articles about (+/-)-Tortuosamine 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: 91.0%

: 159898-43-8
Trifluoro-methanesulfonic acid 6-[2-(benzyl-methyl-amino)-ethyl]-6-(3,4-dimethoxy-phenyl)-5,6-dihydro-quinolin-7-yl ester

: 79517-20-7
(±)-tortuosamine

Guidance literature:: With hydrogen; lithium carbonate; platinum on activated charcoal; In ethanol;
DOI:10.1016/0040-4039(94)88266-5

Reference yield:

: 35135-35-4
(+/-)-sceletium alkaloid A₄

: 79517-20-7
(±)-tortuosamine

Guidance literature:: With hydrogenchloride; hydrogen; palladium on activated charcoal; at 55 ℃; for 42h;
DOI:10.1021/jo00140a003

Reference yield:

: 776-99-8
3,4-dimethoxyphenylacetone

: 79517-20-7
(±)-tortuosamine

Guidance literature:: Multi-step reaction with 4 steps

1: 64 percent / LDA / tetrahydrofuran / -23 °C

2: 83 percent / LDA / tetrahydrofuran / -78 °C

3: 1.) LDA / 1.) THF, 0 deg C, irradiation

4: 91 percent / hydrogen, Li₂CO₃ / Pt/C / ethanol

With hydrogen; lithium carbonate; lithium diisopropyl amide; platinum on activated charcoal; In tetrahydrofuran; ethanol;
DOI:10.1016/0040-4039(94)88266-5