2-(5-fluoro-1H-indol-3-yl)ethanamine;hydron;chloride

Base Information

• Chemical Name: 2-(5-fluoro-1H-indol-3-yl)ethanamine;hydron;chloride
• CAS No.: 2711-58-2
• Molecular Formula: C10H11FN2^.HCl
• Molecular Weight: 214.67
• Hs Code.: 2942000000
• Mol file: 2711-58-2.mol

Synonyms:

Chemical Property of 2-(5-fluoro-1H-indol-3-yl)ethanamine;hydron;chloride

Chemical Property:

• Appearance/Colour: Off white crystalline powder
• Melting Point: 277-283 °C
• Boiling Point: 346 °C at 760 mmHg
• Flash Point: 163 °C
• PSA: 41.81000
• Density: 1.249g/cm3
• LogP: 3.31050
• Storage Temp.: −20°C
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• Exact Mass: 214.0673042
• Heavy Atom Count: 14
• Complexity: 174

Purity/Quality:

99% ^*data from raw suppliers

5-Fluorotryptamine hydrochloride ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: [H+].C1=CC2=C(C=C1F)C(=CN2)CCN.[Cl-]
• Uses: 5-Fluorotryptamine, HCl

Technology Process of 2-(5-fluoro-1H-indol-3-yl)ethanamine;hydron;chloride

There total 1 articles about 2-(5-fluoro-1H-indol-3-yl)ethanamine;hydron;chloride 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:

5-fluorotryptamine (576-16-9) → 5-Fluorotryptamine hydrochloride (2711-58-2)

Guidance literature:

With hydrogenchloride; In diethyl ether; dichloromethane;

DOI:10.1107/S2053229621008950

Reference yield: 83.0%

1-phenyl-5-methyl-1H-1,2,3-triazole-4-carboxylic acid chloride (88958-17-2) + 5-Fluorotryptamine hydrochloride (2711-58-2) → 5-methyl-1-phenyl-N-[2-(5-fluoro-1H-indol-3-yl)ethyl]-1H-1,2,3-triazole-4-carboxamide (1586765-11-8)

Guidance literature:

With potassium carbonate; In dichloromethane; 1,2-dichloro-ethane; at 25 ℃; for 12h;

DOI:10.1134/S1070428014020225

Reference yield: 80.0%

5-Fluorotryptamine hydrochloride (2711-58-2) + 1-tert-butoxycarbonylaminocyclohexanecarboxylic acid (115951-16-1) → tert-butyl 1-(2-(5-fluoro-1H-indol-3-yl)ethylcarbamoyl)cyclohexylcarbamate (1059175-60-8)

Guidance literature:

With N-ethyl-N,N-diisopropylamine; HATU; In N,N-dimethyl-formamide; at 20 ℃; for 18h;

upstream raw materials:

5-fluorotryptamine

Downstream raw materials:

2-[(benzyloxycarbonyl)amino]-isobutyric acid 5-fluorotryptamide

tert-butyl N-[2-(5-fluoro-1H-indol-3-yl)ethyl]carbamate

tert-butyl 1-(2-(5-fluoro-1H-indol-3-yl)ethylcarbamoyl)cyclohexylcarbamate

(E)-3-(3,4-difluorophenyl)-N-(3-(dimethylamino)-1-(2-(5-fluoro-1H-indol-3-yl)ethylamino)-1-oxopropan-2-yl)acrylamide

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