1-benzyl-4-(methoxymethyl)-N-phenylpiperidin-4-amine

  • CasNo:61380-02-7
  • purity:99%
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Details

Factory Supply industrial standard 1-benzyl-4-(methoxymethyl)-N-phenylpiperidin-4-amine 61380-02-7 In Stock

  • Molecular Formula: C20H26 N2 O
  • Molecular Weight: 310.439
  • Vapor Pressure: 1.12E-07mmHg at 25°C 
  • Boiling Point: 432.3°C at 760 mmHg 
  • Flash Point: 215.2°C 
  • PSA: 24.50000 
  • Density: 1.096g/cm3 
  • LogP: 3.79060 

1-benzyl-4-(methoxymethyl)-N-phenylpiperidin-4-amine(Cas 61380-02-7) Usage

InChI:InChI=1/C20H26N2O/c1-23-17-20(21-19-10-6-3-7-11-19)12-14-22(15-13-20)16-18-8-4-2-5-9-18/h2-11,21H,12-17H2,1H3

61380-02-7 Relevant articles

SUBSTITUTED N-(2-(AMINO)-2-OXOETHYL)BENZAMIDE INHIBITORS OF AUTOTAXIN AND THEIR PREPARATION AND USE IN THE TREATMENT OF LPA-DEPENDENT OR LPA-MEDIATED DISEASES

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Page/Page column 36, (2015/12/17)

The present invention relates to compoun...

SUBSTITUTED 4-AMINO-PIPERIDINES

-

Page/Page column 25, (2010/02/17)

The present invention relates to new sub...

A facile method for preparation of [2H3]-sufentanil and its metabolites

Srimurugan, Sankareswaran,Murugan, Kaliyappan,Chen, Chinpiao

experimental part, p. 1421 - 1424 (2010/06/14)

An improved process for the synthesis of...

IMPROVED METHOD OF MAKING SUFENTANIL

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Page/Page column 4; 8-9, (2010/11/29)

The present invention relates to a proce...

61380-02-7 Process route

4-(N-phenylamino)-1-phenylmethyl-4-piperidinylmethanol
61086-04-2

4-(N-phenylamino)-1-phenylmethyl-4-piperidinylmethanol

methyl iodide
74-88-4

methyl iodide

4-(methoxymethyl)-N-phenyl-1-(phenylmethyl)-4-piperidinamine
61380-02-7

4-(methoxymethyl)-N-phenyl-1-(phenylmethyl)-4-piperidinamine

Conditions
Conditions Yield
4-(N-phenylamino)-1-phenylmethyl-4-piperidinylmethanol; With sodium hydride; In tetrahydrofuran; at 20 - 50 ℃;
methyl iodide; In tetrahydrofuran; at 0 - 20 ℃;
83%
4-(N-phenylamino)-1-phenylmethyl-4-piperidinylmethanol; With sodium hydride; In tetrahydrofuran; at 20 ℃; for 2.83333h;
methyl iodide; In tetrahydrofuran; at 20 ℃; for 3.41667h;
80.5%
4-(N-phenylamino)-1-phenylmethyl-4-piperidinylmethanol; With sodium hydride; In tetrahydrofuran; mineral oil; at 20 ℃;
methyl iodide; In tetrahydrofuran; mineral oil; at 20 ℃;
67%
In N,N,N,N,N,N-hexamethylphosphoric triamide; hexane; water; ethyl acetate; mineral oil;
4-(N-phenylamino)-1-phenylmethyl-4-piperidinylmethanol; With sodium hydride; In N,N-dimethyl-formamide; mineral oil; at 0 ℃; for 0.25h;
methyl iodide; In N,N-dimethyl-formamide; mineral oil; for 0.25h;
85 mg
chloroform
67-66-3,8013-54-5

chloroform

N-benzyl-N,N,N-triethylammonium chloride
56-37-1

N-benzyl-N,N,N-triethylammonium chloride

4-(N-phenylamino)-1-phenylmethyl-4-piperidinylmethanol
61086-04-2

4-(N-phenylamino)-1-phenylmethyl-4-piperidinylmethanol

4-(methoxymethyl)-N-phenyl-1-(phenylmethyl)-4-piperidinamine
61380-02-7

4-(methoxymethyl)-N-phenyl-1-(phenylmethyl)-4-piperidinamine

Conditions
Conditions Yield
With sodium hydroxide; dimethyl sulfate; In methanol; water; benzene;
With sodium hydroxide; dimethyl sulfate; In methanol; ice-water; benzene;

61380-02-7 Upstream products

  • 61086-04-2
    61086-04-2

    4-(N-phenylamino)-1-phenylmethyl-4-piperidinylmethanol

  • 74-88-4
    74-88-4

    methyl iodide

  • 67-66-3
    67-66-3

    chloroform

  • 56-37-1
    56-37-1

    N-benzyl-N,N,N-triethylammonium chloride

61380-02-7 Downstream products

  • 61086-12-2
    61086-12-2

    1-benzyl-4-[N-(1-oxopropyl)-N-phenylamino]-4-(methoxymethyl)piperidine

  • 61086-13-3
    61086-13-3

    N-[1-benzyl-4-(methoxymethyl)-4-piperidyl]-N-phenylpropionamide oxalate

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