• Product NameOger hydrochloride
  • CasNo. 87864-14-0
  • MFC16H20 Cl N3 O
  • MW305.807
  • Purity
  • Appearance
  • Packing
  • Contact usInquiry

Product Details

CasNo: 87864-14-0

MF: C16H20 Cl N3 O

Factory supply good quality Oger hydrochloride 87864-14-0 with stock

  • Molecular Formula:C16H20 Cl N3 O
  • Molecular Weight:305.807
  • Vapor Pressure:5.05E-09mmHg at 25°C 
  • Melting Point:65-67°C 
  • Boiling Point:470.5°C at 760 mmHg 
  • PKA:12.77±0.46(Predicted) 
  • Flash Point:238.3°C 
  • PSA:45.23000 
  • Density:1.181g/cm3 
  • LogP:3.35070 

2-Chloro-N-[2-(diethylamino)ethyl]-4-quinolinecarboxamide(Cas 87864-14-0) Usage

InChI:InChI=1/C16H20ClN3O/c1-3-20(4-2)10-9-18-16(21)13-11-15(17)19-14-8-6-5-7-12(13)14/h5-8,11H,3-4,9-10H2,1-2H3,(H,18,21)

87864-14-0 Relevant articles

SMALL MOLECULE ENTEROVIRUS INHIBITORS AND USES THEREOF

-

Paragraph 0093; 0095; 00107-00109; 0124, (2021/08/13)

This invention is in the field of medici...

Identification of dibucaine derivatives as novel potent enterovirus 2C helicase inhibitors: In vitro, in vivo, and combination therapy study

Chen, Yinuo,Feng, Leilei,Jin, Mengyu,Lan, Ke,Shu, Ting,Tang, Qi,Wu, Shuwen,Xu, Zhichao,Zhang, Qiuhan,Zhou, Hai-Bing

, (2020/07/03)

Enterovirus A71 (EV-A71) is a human path...

Quinoline formamide compound and preparation method thereof and application of anti-enterovirus type 71

-

Paragraph 0031-0034, (2020/01/03)

The invention discloses a quinoline form...

Method for preparing N-(2-(diethyl)aminoethyl)-2-chloro-4-quinolinecarboxamide

-

Paragraph 0024-0029, (2019/03/08)

The invention discloses a method for pre...

87864-14-0 Process route

2-chloroquinoline-4-carbonyl chloride
2388-32-1

2-chloroquinoline-4-carbonyl chloride

N,N-diethylethylenediamine
100-36-7

N,N-diethylethylenediamine

2-chloro-quinoline-4-carboxylic acid-(2-diethylamino-ethylamide)
87864-14-0

2-chloro-quinoline-4-carboxylic acid-(2-diethylamino-ethylamide)

Conditions
Conditions Yield
N,N-diethylethylenediamine; With triethylamine; In dichloromethane; for 0.25h; Cooling with ice;
2-chloroquinoline-4-carbonyl chloride; In dichloromethane; at 20 ℃; Cooling with ice;
94%
With chloroform; benzene;
With sodium carbonate; benzene;
With benzene;
With triethylamine; In dichloromethane; at 15 - 20 ℃; for 1.5h;
153.6 g
With triethylamine; In dichloromethane;
2-chloroquinoline-4-carboxylic acid
5467-57-2

2-chloroquinoline-4-carboxylic acid

N,N-diethylethylenediamine
100-36-7

N,N-diethylethylenediamine

2-chloro-quinoline-4-carboxylic acid-(2-diethylamino-ethylamide)
87864-14-0

2-chloro-quinoline-4-carboxylic acid-(2-diethylamino-ethylamide)

Conditions
Conditions Yield
With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In N,N-dimethyl-formamide; at 20 ℃;
82%
2-chloroquinoline-4-carboxylic acid; With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In N,N-dimethyl-formamide; for 0.0333333h; Inert atmosphere;
N,N-diethylethylenediamine; In N,N-dimethyl-formamide; at 20 ℃; Inert atmosphere;
82%

87864-14-0 Upstream products

  • 2388-32-1
    2388-32-1

    2-chloroquinoline-4-carbonyl chloride

  • 100-36-7
    100-36-7

    N,N-diethylethylenediamine

  • 15733-89-8
    15733-89-8

    2-hydroxyquinoline-4-carboxylic acid

  • 5467-57-2
    5467-57-2

    2-chloroquinoline-4-carboxylic acid

87864-14-0 Downstream products

  • 85-79-0
    85-79-0

    Dibucaine

  • 2716-99-6
    2716-99-6

    N-[2-(diethylamino)ethyl]-2-ethoxyquinoline-4-carboxamide

  • 109472-30-2
    109472-30-2

    2-(2-methoxy-ethoxy)-quinoline-4-carboxylic acid-(2-diethylamino-ethylamide)

  • 112248-26-7
    112248-26-7

    N-[2-(diethylamino)ethyl]-2-(2-ethoxyethoxy)quinoline-4-carboxamide

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