FC7Lvp85JZ

Base Information

Chemical Name:FC7Lvp85JZ
CAS No.:189806-34-6
Molecular Formula:C20H22FN3O
Molecular Weight:339.413
Hs Code.:
UNII:FC7LVP85JZ
Nikkaji Number:J1.659.274I
Pharos Ligand ID:AGRZ7XYNHLVB
ChEMBL ID:CHEMBL178066

Synonyms:FC7LVP85JZ;LY-349950 free base;UNII-FC7LVP85JZ;CHEMBL178066;Benzamide, N-(3-(2-(dimethylamino)ethyl)-2-methyl-1H-indol-5-yl)-4-fluoro-;N-(3-(2-(Dimethylamino)ethyl)-2-methyl-1H-indol-5-yl)-4-fluorobenzamide;189806-34-6;SCHEMBL7143303;BDBM50137542;L020893;N-[2-Methyl-3-[2-(dimethylamino)ethyl]-1H-indole-5-yl]-4-fluorobenzamide;N-[3-(2-dimethylamin-oethyl)-2-methyl-1h-indol-5-yl]-4-fluorobenzamide;N-[3-(2-Dimethylamino-ethyl)-2-methyl-1H-indol-5-yl]-4-fluoro-benzamide

Suppliers and Price of FC7Lvp85JZ

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
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price

Total 0 raw suppliers

Chemical Property of FC7Lvp85JZ

Chemical Property:

XLogP3:3.7
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:339.17469050
Heavy Atom Count:25
Complexity:450

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=C(C2=C(N1)C=CC(=C2)NC(=O)C3=CC=C(C=C3)F)CCN(C)C

Technology Process of FC7Lvp85JZ

There total 6 articles about FC7Lvp85JZ 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: 82.0%

: 43018-61-7
1-N,N-dimethylaminopentan-4-one

: 186544-89-8
4-fluoro-N-(4-hydrazino-phenyl)-benzamide

: 189806-34-6
N-[3-(2-dimethylaminoethyl)-2-methyl-1H-indol-5-yl]-4-fluorobenzamide

Guidance literature:: With hydrogenchloride; In ethanol; Heating;
DOI:10.1021/jm0155190

Reference yield: 73.0%

: 189807-12-3
2-methyl-5-amino-3-(2-[N',N'-dimethylamino]ethyl)-1H-indole

: 403-43-0
4-fluorobenzoyl chloride

: 189806-34-6
N-[3-(2-dimethylaminoethyl)-2-methyl-1H-indol-5-yl]-4-fluorobenzamide

Guidance literature:

Reference yield:

: 347-88-6
4-fluoro-N-(4-nitrophenyl)benzamide

: 189806-34-6
N-[3-(2-dimethylaminoethyl)-2-methyl-1H-indol-5-yl]-4-fluorobenzamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: 96 percent / H₂ / Pt/C / tetrahydrofuran / 20 °C

2.1: NaNO₂; HCl

2.2: 60 percent / SnCl₂; HCl

3.1: 82 percent / HCl / ethanol / Heating

With hydrogenchloride; hydrogen; sodium nitrite; platinum on activated charcoal; In tetrahydrofuran; ethanol;
DOI:10.1021/jm0155190