N-allyl-N-methyl-3-hydroxy-7-(2-naphthyl)carbamoyloxy-12-(3,5-dinitriphenyl)carbamoyloxycholan-24-amide

Base Information

Chemical Name:N-allyl-N-methyl-3-hydroxy-7-(2-naphthyl)carbamoyloxy-12-(3,5-dinitriphenyl)carbamoyloxycholan-24-amide
CAS No.:874212-69-8
Molecular Formula:C₄₆H₅₇N₅O₁₀
Molecular Weight:839.986
Hs Code.:

Synonyms:N-allyl-N-methyl-3-hydroxy-7-(2-naphthyl)carbamoyloxy-12-(3,5-dinitriphenyl)carbamoyloxycholan-24-amide

Suppliers and Price of N-allyl-N-methyl-3-hydroxy-7-(2-naphthyl)carbamoyloxy-12-(3,5-dinitriphenyl)carbamoyloxycholan-24-amide

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 N-allyl-N-methyl-3-hydroxy-7-(2-naphthyl)carbamoyloxy-12-(3,5-dinitriphenyl)carbamoyloxycholan-24-amide

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of N-allyl-N-methyl-3-hydroxy-7-(2-naphthyl)carbamoyloxy-12-(3,5-dinitriphenyl)carbamoyloxycholan-24-amide

There total 6 articles about N-allyl-N-methyl-3-hydroxy-7-(2-naphthyl)carbamoyloxy-12-(3,5-dinitriphenyl)carbamoyloxycholan-24-amide 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: 84.0%

: 874212-70-1
Acetic acid (3R,5S,7R,8R,9S,10S,12S,13R,14S,17R)-17-[(R)-3-(allyl-methyl-carbamoyl)-1-methyl-propyl]-12-(3,5-dinitro-phenylcarbamoyloxy)-10,13-dimethyl-7-(naphthalen-2-ylcarbamoyloxy)-hexadecahydro-cyclopenta[a]phenanthren-3-yl ester

: 874212-69-8
N-allyl-N-methyl-3-hydroxy-7-(2-naphthyl)carbamoyloxy-12-(3,5-dinitriphenyl)carbamoyloxycholan-24-amide

Guidance literature:: With hydrogenchloride; In methanol; for 1h; Heating;
DOI:10.1016/j.tetasy.2005.10.036

Reference yield:

: 874212-76-7
Acetic acid (3R,5S,8R,9S,10S,12S,13R,14S,17R)-17-[(R)-3-(allyl-methyl-carbamoyl)-1-methyl-propyl]-12-hydroxy-10,13-dimethyl-7-oxo-hexadecahydro-cyclopenta[a]phenanthren-3-yl ester

: 874212-69-8
N-allyl-N-methyl-3-hydroxy-7-(2-naphthyl)carbamoyloxy-12-(3,5-dinitriphenyl)carbamoyloxycholan-24-amide

Guidance literature:: Multi-step reaction with 4 steps

1: 80 percent / toluene / Heating

2: 81 percent / NaBH₄ / tetrahydrofuran; methanol / 0 - 20 °C

3: 74 percent / DMAP / toluene / 24 h / Heating

4: 84 percent / HCl / methanol / 1 h / Heating

With hydrogenchloride; dmap; sodium tetrahydroborate; In tetrahydrofuran; methanol; toluene;
DOI:10.1016/j.tetasy.2005.10.036

Reference yield:

: 874212-72-3
Acetic acid (3R,5R,7R,8R,9S,10S,12S,13R,14S,17R)-17-[(R)-3-(allyl-methyl-carbamoyl)-1-methyl-propyl]-12-(3,5-dinitro-phenylcarbamoyloxy)-7-hydroxy-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-3-yl ester

: 874212-69-8
N-allyl-N-methyl-3-hydroxy-7-(2-naphthyl)carbamoyloxy-12-(3,5-dinitriphenyl)carbamoyloxycholan-24-amide

Guidance literature:: Multi-step reaction with 2 steps

1: 74 percent / DMAP / toluene / 24 h / Heating

2: 84 percent / HCl / methanol / 1 h / Heating

With hydrogenchloride; dmap; In methanol; toluene;
DOI:10.1016/j.tetasy.2005.10.036