6-Chloro-4-cyclopropylquinazolin-2(1H)-one

Base Information

• Chemical Name: 6-Chloro-4-cyclopropylquinazolin-2(1H)-one
• CAS No.: 150878-36-7
• Molecular Formula: C11H9ClN2O
• Molecular Weight: 220.658
• Hs Code.: 2933990090
• DSSTox Substance ID: DTXSID20438583
• Wikidata: Q72518174
• Mol file: 150878-36-7.mol

Synonyms:150878-36-7;6-Chloro-4-cyclopropylquinazolin-2(1H)-one;6-chloro-4-cyclopropyl-3H-quinazolin-2-one;6-chloro-4-cyclopropyl-1,2-dihydroquinazolin-2-one;2(1H)-Quinazolinone, 6-chloro-4-cyclopropyl-;SCHEMBL9115314;DTXSID20438583;MKYOBEYCYMHIKA-UHFFFAOYSA-N;MFCD11109434;AKOS015850492;6-Chloro-4-cyclopropylquinazolin-2-ol;PS-3962;CS-0447092;FT-0685542;A884129;6-Chloro-4-cyclopropylquinazolin-2(1H)-one 95+%

Chemical Property of 6-Chloro-4-cyclopropylquinazolin-2(1H)-one

Chemical Property:

• PSA: 45.75000
• Density: 1.57
• LogP: 2.45390
• XLogP3: 1.5
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 220.0403406
• Heavy Atom Count: 15
• Complexity: 467

Purity/Quality:

97% ^*data from raw suppliers

6-Chloro-4-cyclopropylquinazolin-2(1H)-one 95.0% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1CC1C2=C3C=C(C=CC3=NC(=O)N2)Cl

Technology Process of 6-Chloro-4-cyclopropylquinazolin-2(1H)-one

There total 5 articles about 6-Chloro-4-cyclopropylquinazolin-2(1H)-one 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:

cyclopropyl bromide (4333-56-6,130561-87-4) + 2-amino-5-chlorobenzonitrile (5922-60-1) + carbonic acid dimethyl ester (616-38-6) → 6-chloro-4-cyclopropylquinazolin-2(1H)-one (150878-36-7)

Guidance literature:

With citric acid; In tetrahydrofuran;

Reference yield:

potassium cyanate (590-28-3) + cyclopropyl (4-chloroanilin-2-yl)-ketone (150879-49-5) → 6-chloro-4-cyclopropylquinazolin-2(1H)-one (150878-36-7) + N-(4-Chloro-2-cyclopropanecarbonyl-phenyl)-acetamide

Guidance literature:

With acetic acid; In water; Yield given. Yields of byproduct given;

DOI:10.1016/0040-4039(94)85011-9

Reference yield:

potassium cyanate (590-28-3) + acetic acid (64-19-7,77671-22-8) + cyclopropyl (4-chloroanilin-2-yl)-ketone (150879-49-5) → 6-chloro-4-cyclopropylquinazolin-2(1H)-one (150878-36-7) + N-(4-Chloro-2-cyclopropanecarbonyl-phenyl)-acetamide

Guidance literature:

With potassium cyanate; In water; Yield given. Yields of byproduct given;

DOI:10.1016/0040-4039(94)85011-9

upstream raw materials:

potassium cyanate

cyclopropyl (4-chloroanilin-2-yl)-ketone

acetic acid

2-amino-5-chlorobenzonitrile

Downstream raw materials:

6-chloro-4-cyclopropyl-1-(4-methoxybenzyl)-4-(4-methoxybutynyl)-3-(2-methoxyethyl)-3,4-dihydroquinazolin-2(1H)-one

3,4-dihydro-1-(4-methoxybenzyl)-4-cyclopropyl-4-(2-butyn-1-yl)-6-chloroquinazolin-2(1H)one

(+/-)-6-Chloro-4-cyclopropyl-3,4-dihydro-1-(4-methoxybenzyl)-4-n-butylquinazolin-2(1H)-one

6-chloro-4-cyclopropyl-1-(4-methoxybenzyl)-quinazolin-2(1H)-one