leuconolam methyl ether

Base Information

Chemical Name:leuconolam methyl ether
CAS No.:109305-79-5
Molecular Formula:C₂₀H₂₄N₂O₃
Molecular Weight:340.422
Hs Code.:

Synonyms:

Suppliers and Price of leuconolam methyl ether

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 leuconolam methyl ether

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of leuconolam methyl ether

There total 3 articles about leuconolam methyl ether 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: 94.0%

: 67-56-1
methanol

: 93710-27-1,109363-24-8
(?)-leuconolam

: 1538555-29-1
(+)-11-(2-aminophenyl)-4a-ethyl-3,4,4a,5,6,7-hexahydropyrano[3,2-h]indolizine-2,9-dione

: 109305-79-5
leuconolam methyl ether

Guidance literature:: With camphor-10-sulfonic acid; at 20 ℃; for 12h; Reagent/catalyst; Inert atmosphere;
DOI:10.1021/np400922x

Reference yield:

: 6,7-dehydroleuconoxine

: 1538555-29-1
(+)-11-(2-aminophenyl)-4a-ethyl-3,4,4a,5,6,7-hexahydropyrano[3,2-h]indolizine-2,9-dione

: 109305-79-5
leuconolam methyl ether

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogenchloride; tetraethylammonium chloride / dichloromethane; water / 12 h / 20 °C

2: camphor-10-sulfonic acid / 12 h / 20 °C / Inert atmosphere

With hydrogenchloride; camphor-10-sulfonic acid; tetraethylammonium chloride; In dichloromethane; water;
DOI:10.1021/np400922x

Reference yield:

: 128529-80-6
6β,7β-dibromodiazaspiroleuconolam

: 1538555-29-1
(+)-11-(2-aminophenyl)-4a-ethyl-3,4,4a,5,6,7-hexahydropyrano[3,2-h]indolizine-2,9-dione

: 109305-79-5
leuconolam methyl ether

Guidance literature:: Multi-step reaction with 3 steps

1: acetic acid; zinc / 2 h / Inert atmosphere

2: hydrogenchloride; tetraethylammonium chloride / dichloromethane; water / 12 h / 20 °C

3: camphor-10-sulfonic acid / 12 h / 20 °C / Inert atmosphere

With hydrogenchloride; camphor-10-sulfonic acid; tetraethylammonium chloride; acetic acid; zinc; In dichloromethane; water;
DOI:10.1021/np400922x