5H-Pyrido(4,3-b)indol-3-amine, 1-ethyl-, monoacetate

Base Information

Chemical Name:5H-Pyrido(4,3-b)indol-3-amine, 1-ethyl-, monoacetate
CAS No.:75240-10-7
Molecular Formula:C₂H₄O₂*C₁₃H₁₃N₃
Molecular Weight:271.319
Hs Code.:
DSSTox Substance ID:DTXSID40226222

Synonyms:5H-Pyrido(4,3-b)indol-3-amine, 1-ethyl-, monoacetate;75240-10-7;DTXSID40226222

Suppliers and Price of 5H-Pyrido(4,3-b)indol-3-amine, 1-ethyl-, monoacetate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Chemical Property of 5H-Pyrido(4,3-b)indol-3-amine, 1-ethyl-, monoacetate

Chemical Property:

Vapor Pressure:1.68E-08mmHg at 25°C
Boiling Point:456°Cat760mmHg
Flash Point:260.3°C
Density:g/cm³
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:1
Exact Mass:271.132076794
Heavy Atom Count:20
Complexity:287

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCC1=C2C3=CC=CC=C3NC2=CC(=N1)N.CC(=O)O

Technology Process of 5H-Pyrido(4,3-b)indol-3-amine, 1-ethyl-, monoacetate

There total 3 articles about 5H-Pyrido(4,3-b)indol-3-amine, 1-ethyl-, monoacetate 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: 27.0%

: 7210-27-7
2-indoleacetonitrile

: 64-19-7,77671-22-8
acetic acid

: 107-12-0
propiononitrile

: 75240-10-7
1-Ethyl-5H-pyrido[4,3-b]indol-3-ylamine; compound with acetic acid

Guidance literature:: aluminium trichloride; at 100 - 120 ℃; for 12h;
DOI:10.1248/cpb.29.1280

Reference yield:

: 52618-53-8
2-(cyanomethyl)-N-ethoxycarbonylindole

: 75240-10-7
1-Ethyl-5H-pyrido[4,3-b]indol-3-ylamine; compound with acetic acid

Guidance literature:: Multi-step reaction with 2 steps

1: K₂CO₃ / methanol / 0 °C

2: 27 percent / aluminum chloride / 12 h / 100 - 120 °C

With potassium carbonate; aluminium trichloride; In methanol;
DOI:10.1248/cpb.29.1280

Reference yield:

: 17954-23-3
1-ethoxycarbonyl-1,2-dihydroquinoline-2-carbonitrile

: 75240-10-7
1-Ethyl-5H-pyrido[4,3-b]indol-3-ylamine; compound with acetic acid

Guidance literature:: Multi-step reaction with 3 steps

1: Irradiation

2: K₂CO₃ / methanol / 0 °C

3: 27 percent / aluminum chloride / 12 h / 100 - 120 °C

With potassium carbonate; aluminium trichloride; In methanol;
DOI:10.1248/cpb.29.1280