2-(5-Aminopentyl)isoindoline-1,3-dione hydrochloride

Base Information

• Chemical Name: 2-(5-Aminopentyl)isoindoline-1,3-dione hydrochloride
• CAS No.: 7292-63-9
• Molecular Formula: C13H16N2O2
• Molecular Weight: 268.743
• Hs Code.: 2925190090
• DSSTox Substance ID: DTXSID90590445
• NSC Number: 159714
• Mol file: 7292-63-9.mol

Synonyms:7292-63-9;2-(5-Aminopentyl)isoindoline-1,3-dione hydrochloride;n-(5-amino-pentyl)-phthalimide hcl;2-(5-aminopentyl)isoindole-1,3-dione;hydrochloride;MFCD08448237;N-(5-Aminopentyl)phthalimide hydrochloride;N-(5-Aminopentyl)phthalimide, hydrochloride;SCHEMBL11628370;DTXSID90590445;NSC159714;AKOS015996058;N-(5-Amino-pentyl)-phthalimide x HCl;NSC-159714;SB64840;MS-21694;n-(5-aminopentyl)-phthalimidehydrochloride;DB-055698;CS-0326502;n-(5-amino-pentyl)-phthalimide hydrochloride;N-(5-Aminopentyl)-phthalimide, hydrochloride;A837670;A1-04494;2-(5-Aminopentyl)-1H-isoindole-1,3(2H)-dione--hydrogen chloride (1/1)

Chemical Property of 2-(5-Aminopentyl)isoindoline-1,3-dione hydrochloride

Chemical Property:

• Vapor Pressure: 4.96E-07mmHg at 25°C
• Boiling Point: 407.3°C at 760 mmHg
• Flash Point: 200.1°C
• PSA: 63.40000
• LogP: 2.85180
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 5
• Exact Mass: 268.0978555
• Heavy Atom Count: 18
• Complexity: 280

Purity/Quality:

97% ^*data from raw suppliers

2-(5-Aminopentyl)-2,3-dihydro-1H-isoindole-1,3-dione hydrochloride 98.0% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C2C(=C1)C(=O)N(C2=O)CCCCCN.Cl

Technology Process of 2-(5-Aminopentyl)isoindoline-1,3-dione hydrochloride

There total 5 articles about 2-(5-Aminopentyl)isoindoline-1,3-dione hydrochloride 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: 92.0%

2-(5-azidopentyl)isoindoline-1,3-dione → N-(5-aminopentyl)phthalimide hydrochloride (7292-63-9)

Guidance literature:

With palladium 10% on activated carbon; hydrogen; acetic acid; In methanol; for 12h; under 25858.1 Torr;

Reference yield:

potassium phtalimide (1074-82-4) → N-(5-aminopentyl)phthalimide hydrochloride (7292-63-9)

Guidance literature:

Multi-step reaction with 3 steps

1: potassium carbonate / acetonitrile / 24 h / Reflux

2: potassium carbonate / acetonitrile / Reflux

3: hydrazine hydrate; hydrochloric acid diethyl ether / ethanol / Reflux

With hydrochloric acid diethyl ether; potassium carbonate; hydrazine hydrate; In ethanol; acetonitrile;

DOI:10.1021/acs.molpharmaceut.9b00075

Reference yield:

1,5-dibromo-pentane (111-24-0) → N-(5-aminopentyl)phthalimide hydrochloride (7292-63-9)

Guidance literature:

Multi-step reaction with 3 steps

1: potassium carbonate / acetonitrile / 24 h / Reflux

2: potassium carbonate / acetonitrile / Reflux

3: hydrazine hydrate; hydrochloric acid diethyl ether / ethanol / Reflux

With hydrochloric acid diethyl ether; potassium carbonate; hydrazine hydrate; In ethanol; acetonitrile;

DOI:10.1021/acs.molpharmaceut.9b00075

upstream raw materials:

potassium phtalimide

1,5-dibromo-pentane

N-(5-bromopentyl)phthalimide

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