(E)-N-{2-[1-benzyl-2-(3-hydroxyprop-1-en-1-yl)-5-methoxy-1H-indol-3-yl]ethyl}-2,2,2-trifluoroacetamide

Base Information

Chemical Name:(E)-N-{2-[1-benzyl-2-(3-hydroxyprop-1-en-1-yl)-5-methoxy-1H-indol-3-yl]ethyl}-2,2,2-trifluoroacetamide
CAS No.:1369852-97-0
Molecular Formula:C₂₃H₂₃F₃N₂O₃
Molecular Weight:432.442
Hs Code.:

Synonyms:(E)-N-{2-[1-benzyl-2-(3-hydroxyprop-1-en-1-yl)-5-methoxy-1H-indol-3-yl]ethyl}-2,2,2-trifluoroacetamide

Suppliers and Price of (E)-N-{2-[1-benzyl-2-(3-hydroxyprop-1-en-1-yl)-5-methoxy-1H-indol-3-yl]ethyl}-2,2,2-trifluoroacetamide

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 (E)-N-{2-[1-benzyl-2-(3-hydroxyprop-1-en-1-yl)-5-methoxy-1H-indol-3-yl]ethyl}-2,2,2-trifluoroacetamide

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (E)-N-{2-[1-benzyl-2-(3-hydroxyprop-1-en-1-yl)-5-methoxy-1H-indol-3-yl]ethyl}-2,2,2-trifluoroacetamide

There total 5 articles about (E)-N-{2-[1-benzyl-2-(3-hydroxyprop-1-en-1-yl)-5-methoxy-1H-indol-3-yl]ethyl}-2,2,2-trifluoroacetamide 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: 68.0%

: 1369852-86-7
N-[2-(1-benzyl-2-iodo-5-methoxy-1H-indol-3-yl)ethyl]-2,2,2-trifluoroacetamide

: 82994-41-0,81925-29-3,74141-12-1,74141-13-2
(E)-3-(tri-n-butylstannyl)-2-propen-1-ol

: 1369852-97-0
(E)-N-{2-[1-benzyl-2-(3-hydroxyprop-1-en-1-yl)-5-methoxy-1H-indol-3-yl]ethyl}-2,2,2-trifluoroacetamide

Guidance literature:: With bis-triphenylphosphine-palladium(II) chloride; lithium chloride; In N,N-dimethyl-formamide; at 75 ℃; for 16h; Inert atmosphere;
DOI:10.1055/s-0031-1289656

Reference yield:

: 1369852-63-0
N-[2-(1-benzyl-5-methoxy-1H-indol-3-yl)ethyl]-2,2,2-trifluoroacetamide

: 1369852-97-0
(E)-N-{2-[1-benzyl-2-(3-hydroxyprop-1-en-1-yl)-5-methoxy-1H-indol-3-yl]ethyl}-2,2,2-trifluoroacetamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: n-butyllithium / diethyl ether; hexane / 2 h / 0 - 20 °C / Inert atmosphere

1.2: 0 - 20 °C / Inert atmosphere

2.1: bis-triphenylphosphine-palladium(II) chloride; lithium chloride / N,N-dimethyl-formamide / 16 h / 75 °C / Inert atmosphere

With bis-triphenylphosphine-palladium(II) chloride; n-butyllithium; lithium chloride; In diethyl ether; hexane; N,N-dimethyl-formamide; 2.1: Stille coupling;
DOI:10.1055/s-0031-1289656

Reference yield:

: 100-39-0
benzyl bromide

: 1369852-97-0
(E)-N-{2-[1-benzyl-2-(3-hydroxyprop-1-en-1-yl)-5-methoxy-1H-indol-3-yl]ethyl}-2,2,2-trifluoroacetamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium hydride / N,N-dimethyl-formamide / 0.5 h / 50 °C / Inert atmosphere

1.2: 1 h / 50 °C / Inert atmosphere

2.1: pyridine / dichloromethane / 16 h / 0 - 20 °C / Inert atmosphere

3.1: n-butyllithium / diethyl ether; hexane / 2 h / 0 - 20 °C / Inert atmosphere

3.2: 0 - 20 °C / Inert atmosphere

4.1: bis-triphenylphosphine-palladium(II) chloride; lithium chloride / N,N-dimethyl-formamide / 16 h / 75 °C / Inert atmosphere

With pyridine; bis-triphenylphosphine-palladium(II) chloride; n-butyllithium; sodium hydride; lithium chloride; In diethyl ether; hexane; dichloromethane; N,N-dimethyl-formamide; 4.1: Stille coupling;
DOI:10.1055/s-0031-1289656