1-TERT-BUTYL-PIPERIDIN-4-ONE


  • CAS 1465-76-5
  • Purity 99%
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Cost-effective and customizable 1-TERT-BUTYL-PIPERIDIN-4-ONE 1465-76-5 factory

  • Molecular Formula: C9H17NO
  • Molecular Weight: 155.24
  • Vapor Pressure: 0.0883mmHg at 25°C 
  • Melting Point: 92-94 °C (sublm)(Press: 10 Torr) 
  • Refractive Index: 1.472 
  • Boiling Point: 225 °C at 760 mmHg 
  • PKA: 8.26±0.20(Predicted) 
  • Flash Point: 83.5 °C 
  • PSA: 20.31000 
  • Density: 0.968 g/cm3 
  • LogP: 1.38770 

1-TERT-BUTYL-PIPERIDIN-4-ONE(Cas 1465-76-5) Usage

General Description

1-TERT-BUTYL-PIPERIDIN-4-ONE is a key intermediate in the synthesis of pharmaceutical compounds, such as p38 MAP kinase inhibitors, where it serves as a precursor for Grignard reactions. Its efficient preparation via transamination is facilitated by trapping dimethylamine with sodium acrylate, enabling high-yield production and simplified purification. 1-TERT-BUTYL-PIPERIDIN-4-ONE is particularly valuable in large-scale drug synthesis, as demonstrated in the development of therapeutics for rheumatoid arthritis and psoriasis.

InChI:InChI=1/C9H17NO/c1-9(2,3)10-6-4-8(11)5-7-10/h4-7H2,1-3H3

1465-76-5 Relevant articles

Acrylate as an efficient dimethylamine trap for the practical synthesis of 1-tert-butyl-4-piperidone via transamination

Amato, Joseph S.,Chung, John Y. L.,Cvetovich, Raymond J.,Reamer, Robert A.,Zhao, Dalian,Zhou, George,Gong, Xiaoyi

, p. 939 - 941 (2004)

Efficient trapping of dimethylamine was ...

Synthesis of a naphthyridone p38 MAP kinase inhibitor

Chung, John Y. L.,Cvetovich, Raymond J.,McLaughlin, Mark,Amato, Joseph,Tsay, Fuh-Rong,Jensen, Mark,Weissman, Steve,Zewge, Daniel

, p. 8602 - 8609 (2006)

Compound 1 is a p38 MAP kinase inhibitor...

Fused tricyclic hepatitis virus inhibitor and application thereof

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Paragraph 0696; 0697; 0698; 0699; 0700, (2016/12/26)

The invention belongs to the field of me...

AZACYCLIC COMPOUNDS

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Paragraph 0666, (2015/11/09)

Compounds and methods are provided for t...

Spiroalkene carboxamide derivatives and their use as chemokine receptor modulators

-

Page/Page column 53, (2012/10/18)

The present invention is directed to com...

SPIROALKENE CARBOXAMIDE DERIVATIVES AND THEIR USE AS CHEMOKINE RECEPTOR MODULATORS

-

Page/Page column 64, (2012/10/18)

The present invention is directed to com...

1465-76-5 Process route

1-methyl-1-ethyl-4-oxopiperidinium iodide
77542-18-8

1-methyl-1-ethyl-4-oxopiperidinium iodide

<i>tert</i>-butylamine
75-64-9

tert -butylamine

1-tert-butyl-piperidin-4-one
1465-76-5

1-tert-butyl-piperidin-4-one

Conditions
Conditions Yield
With sodium hydrogencarbonate; In water; toluene; at 0 - 80 ℃; for 5h;
37%
With sodium hydrogencarbonate; In water; toluene; at 0 - 80 ℃; for 5h;
37%
With sodium hydrogencarbonate; In water; toluene; at 78 ℃; for 6h;
With sodium hydrogencarbonate; In water; toluene; at 78 ℃; for 6h;
N,N-dimethyl-4-oxopiperidinium iodide
26822-37-7

N,N-dimethyl-4-oxopiperidinium iodide

<i>tert</i>-butylamine
75-64-9

tert -butylamine

1-tert-butyl-piperidin-4-one
1465-76-5

1-tert-butyl-piperidin-4-one

Conditions
Conditions Yield
With sodium 2-propenoate; In water;
87%
With sodium hydroxide; acrylic acid; In water; at 65 ℃; for 3h; Inert atmosphere;
75%
N,N-dimethyl-4-oxopiperidinium iodide; tert-butylamine; In water; for 0.25h;
With N-benzyl-trimethylammonium hydroxide; In methanol; water; for 2h; Heating / reflux;
With sodium hydroxide; In water;
With acrylic acid; sodium hydroxide; In water; at 80 ℃; for 3h;

1465-76-5 Upstream products

  • 1445-73-4
    1445-73-4

    1-Methyl-4-piperidone

  • 75-64-9
    75-64-9

    tert -butylamine

  • 26822-37-7
    26822-37-7

    N,N-dimethyl-4-oxopiperidinium iodide

  • 77542-18-8
    77542-18-8

    1-methyl-1-ethyl-4-oxopiperidinium iodide

1465-76-5 Downstream products

  • 57982-78-2
    57982-78-2

    budipine

  • 5382-30-9
    5382-30-9

    1-(1,1-dimethylethyl)-4-piperidinol

  • 359880-72-1
    359880-72-1

    4-(4-methylbenzylamino)-1-tert-butylpiperidine

  • 844443-82-9
    844443-82-9

    N-benzyl-1-tert-butylpiperidin-4-amine

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