4-bromo-N-((3R,5aS,6R,8aS,9R,12R,12aR)-3,6,9-trimethyl-10-oxodecahydro-3,12-epoxy[1,2]dioxepino[4,3-i]isoquinolin-11(12H)-yl)benzamide

Base Information

Chemical Name:4-bromo-N-((3R,5aS,6R,8aS,9R,12R,12aR)-3,6,9-trimethyl-10-oxodecahydro-3,12-epoxy[1,2]dioxepino[4,3-i]isoquinolin-11(12H)-yl)benzamide
CAS No.:1086409-89-3
Molecular Formula:C₂₂H₂₇BrN₂O₅
Molecular Weight:479.371
Hs Code.:

Synonyms:4-bromo-N-((3R,5aS,6R,8aS,9R,12R,12aR)-3,6,9-trimethyl-10-oxodecahydro-3,12-epoxy[1,2]dioxepino[4,3-i]isoquinolin-11(12H)-yl)benzamide

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Chemical Property of 4-bromo-N-((3R,5aS,6R,8aS,9R,12R,12aR)-3,6,9-trimethyl-10-oxodecahydro-3,12-epoxy[1,2]dioxepino[4,3-i]isoquinolin-11(12H)-yl)benzamide

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Technology Process of 4-bromo-N-((3R,5aS,6R,8aS,9R,12R,12aR)-3,6,9-trimethyl-10-oxodecahydro-3,12-epoxy[1,2]dioxepino[4,3-i]isoquinolin-11(12H)-yl)benzamide

There total 2 articles about 4-bromo-N-((3R,5aS,6R,8aS,9R,12R,12aR)-3,6,9-trimethyl-10-oxodecahydro-3,12-epoxy[1,2]dioxepino[4,3-i]isoquinolin-11(12H)-yl)benzamide 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: 60.0%

: 1086409-78-0
(3R,5aS,6R,8aS,9R,12R,12aR)-11-amino-3,6,9-trimethyldecahydro-3,12-epoxy[1,2]dioxepino[4,3-i]isoquinolin-10(3H)-one

: 586-75-4
4-chlorobenzoyl chloride

: 1086409-89-3
4-bromo-N-((3R,5aS,6R,8aS,9R,12R,12aR)-3,6,9-trimethyl-10-oxodecahydro-3,12-epoxy[1,2]dioxepino[4,3-i]isoquinolin-11(12H)-yl)benzamide

Guidance literature:: With triethylamine; In benzene; at 0 ℃; for 2h;
DOI:10.1021/ol802238d

Reference yield:

: 63968-64-9
C₁₂H₁₃O₂(CH₃)3(O)(OO)

: 1086409-89-3
4-bromo-N-((3R,5aS,6R,8aS,9R,12R,12aR)-3,6,9-trimethyl-10-oxodecahydro-3,12-epoxy[1,2]dioxepino[4,3-i]isoquinolin-11(12H)-yl)benzamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: hydrazine hydrate / methanol; chloroform / 1.08 h / 0 °C

1.2: 12 h / 20 °C

2.1: triethylamine / benzene / 2 h / 0 °C

With hydrazine hydrate; triethylamine; In methanol; chloroform; benzene;
DOI:10.1021/jm401774f