N-(6-methylquinolin-2-yl)acetamide

Base Information

Chemical Name:N-(6-methylquinolin-2-yl)acetamide
CAS No.:863549-39-7
Molecular Formula:C₁₂H₁₂N₂O
Molecular Weight:200.24
Hs Code.:
DSSTox Substance ID:DTXSID601298151

Synonyms:863549-39-7;N-(6-methylquinolin-2-yl)acetamide;2-(Acetamido)-6-methylquinoline;SCHEMBL15450991;LQTGYIFEQTXQFX-UHFFFAOYSA-N;DTXSID601298151;N-(6-Methyl-2-quinolinyl)acetamide

Suppliers and Price of N-(6-methylquinolin-2-yl)acetamide

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
Packaging
price

Total 0 raw suppliers

Chemical Property of N-(6-methylquinolin-2-yl)acetamide

Chemical Property:

XLogP3:2.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:200.094963011
Heavy Atom Count:15
Complexity:242

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=CC2=C(C=C1)N=C(C=C2)NC(=O)C

Technology Process of N-(6-methylquinolin-2-yl)acetamide

There total 1 articles about N-(6-methylquinolin-2-yl)acetamide 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: 68.0%

: 60-35-5
acetamide

: 4295-11-8
2-chloro-6-methylquinoline

: 863549-39-7
N-(6-methylquinolin-2-yl)acetamide

: 20150-84-9
2-amino-6-methylquinoline

: 4053-34-3
6-methylquinolin-2(1H)-one

Guidance literature:: With potassium carbonate; for 15h; Heating;
DOI:10.1039/b504498g

Reference yield:

: 863549-39-7
N-(6-methylquinolin-2-yl)acetamide

: 1562370-49-3
C₂₁H₂₂FN₃O

Guidance literature:: Multi-step reaction with 4 steps

1.1: N-Bromosuccinimide; dibenzoyl peroxide / benzene / 2.67 h / Inert atmosphere; Reflux

2.1: N,N-dimethyl-formamide / 17 h / 20 °C

3.1: hydrogen; ammonia / methanol; ethanol / 0.5 h

4.1: acetic acid; magnesium sulfate / methanol; chloroform / 0.33 h / 20 °C

4.2: 0.83 h / 0 - 20 °C

With N-Bromosuccinimide; ammonia; hydrogen; magnesium sulfate; acetic acid; dibenzoyl peroxide; In methanol; ethanol; chloroform; N,N-dimethyl-formamide; benzene;
DOI:10.1021/jm401838x

Reference yield:

: 863549-39-7
N-(6-methylquinolin-2-yl)acetamide

: 1562370-51-7
C₂₂H₂₄FN₃O

Guidance literature:: Multi-step reaction with 4 steps

1.1: N-Bromosuccinimide; dibenzoyl peroxide / benzene / 2.67 h / Inert atmosphere; Reflux

2.1: N,N-dimethyl-formamide / 17 h / 20 °C

3.1: hydrogen; ammonia / methanol; ethanol / 0.5 h

4.1: acetic acid; magnesium sulfate / methanol; chloroform / 0.42 h / 20 °C

4.2: 0.5 h / 0 - 20 °C

With N-Bromosuccinimide; ammonia; hydrogen; magnesium sulfate; acetic acid; dibenzoyl peroxide; In methanol; ethanol; chloroform; N,N-dimethyl-formamide; benzene;
DOI:10.1021/jm401838x