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[ CAS No. 64690-19-3 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 64690-19-3
Chemical Structure| 64690-19-3
Structure of 64690-19-3 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 64690-19-3 ]

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Product Details of [ 64690-19-3 ]

CAS No. :64690-19-3 MDL No. :MFCD09743883
Formula : C13H22N2 Boiling Point : -
Linear Structure Formula :- InChI Key :RHDWCSIBVZKRRU-UHFFFAOYSA-N
M.W : 206.33 Pubchem ID :3017535
Synonyms :

Calculated chemistry of [ 64690-19-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 15
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.62
Num. rotatable bonds : 8
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 67.19
TPSA : 24.92 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : No
CYP2D6 inhibitor : Yes
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -4.54 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.94
Log Po/w (XLOGP3) : 4.25
Log Po/w (WLOGP) : 3.66
Log Po/w (MLOGP) : 2.28
Log Po/w (SILICOS-IT) : 3.47
Consensus Log Po/w : 3.32

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 0.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -3.56
Solubility : 0.0562 mg/ml ; 0.000272 mol/l
Class : Soluble
Log S (Ali) : -4.48
Solubility : 0.00676 mg/ml ; 0.0000328 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -5.3
Solubility : 0.00103 mg/ml ; 0.00000498 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 3.0
Synthetic accessibility : 1.67

Safety of [ 64690-19-3 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P280-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H332-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 64690-19-3 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Upstream synthesis route of [ 64690-19-3 ]

[ 64690-19-3 ] Synthesis Path-Upstream   1~8

  • 1
  • [ 504-24-5 ]
  • [ 124-13-0 ]
  • [ 64690-19-3 ]
Reference: [1] Journal of Medicinal Chemistry, 1984, vol. 27, # 11, p. 1457 - 1464
[2] Patent: US4206215, 1980, A,
  • 2
  • [ 111-86-4 ]
  • [ 19524-06-2 ]
  • [ 64690-19-3 ]
Reference: [1] Journal of the American Chemical Society, 2008, vol. 130, # 20, p. 6586 - 6596
[2] Organic Letters, 2008, vol. 10, # 18, p. 4109 - 4112
  • 3
  • [ 111-86-4 ]
  • [ 7379-35-3 ]
  • [ 64690-19-3 ]
YieldReaction ConditionsOperation in experiment
78.5% at 130℃; for 2 h; Large scale Into 200L reactor was pumped n-octylamine 100kg,30kg of 4-chloropyridine hydrochloride and 10kg of sodium fluoride were added, the temperature was raised to 130 ° C, and the mixture was stirred for 2 hours while keeping warm,Decompression recovery n-octylamine, while hot sodium carbonate aqueous solution to adjust the pH to about 7, adding ethyl acetate 120kg, separating the aqueous layer, the organic layer was cooled, filtered,Dried to give 4-octylaminopyridine 32.3kg,Purity was 99.3percent, yield was 78.5percent.
Reference: [1] Journal of the American Chemical Society, 2008, vol. 130, # 20, p. 6586 - 6596
[2] Patent: CN107501173, 2017, A, . Location in patent: Paragraph 0018
  • 4
  • [ 111-86-4 ]
  • [ 36316-71-9 ]
  • [ 64690-19-3 ]
Reference: [1] Angewandte Chemie - International Edition, 2005, vol. 44, # 9, p. 1371 - 1375
  • 5
  • [ 15854-87-2 ]
  • [ 111-86-4 ]
  • [ 64690-19-3 ]
Reference: [1] Journal of the American Chemical Society, 2008, vol. 130, # 20, p. 6586 - 6596
  • 6
  • [ 142-95-0 ]
  • [ 7379-35-3 ]
  • [ 64690-19-3 ]
YieldReaction ConditionsOperation in experiment
93% at 120 - 200℃; for 7 h; 5.0 g (0.0333 mol) of 4-chlororpyridine hydrochloride,And 0.55 g (0.0333 mol) of n-OCtylaminehydrochloride,The mixture is stirred and heated from 120 ° C to 180 ° C, heated to 200 ° C and held for 7 hours. The reaction was confirmed by thin-layer chromatography, and after completion, it was cooled and cooled to 100 ° C. To the reaction solution was added 20 ml of water and the mixture was cooled with stirring.To the reaction mixture was added 35percent aqueous solution of sodium hydroxide to make it alkaline. The mixture was extracted three times with 20 ml of di-dichloromethane (MC). The organic layer was collected, washed with 10 ml of cold water, washed with saturated brine, dehydrated with magnesium sulfate and filtered. The filtrate was evaporated under reduced pressure, 14 ml of hexane was added to the residue solid, and the mixture was refluxed and cooled. The resulting crystals were filtered, dried under reduced pressure at room temperature. [0103] 6.4 g of octylaminopyridine base (yield: 93.0percent, MP 65-69 ° C) was obtained through the above-mentioned procedure.
Reference: [1] Patent: KR2017/13425, 2017, A, . Location in patent: Paragraph 0099; 0100
[2] Patent: US4206215, 1980, A,
  • 7
  • [ 626-61-9 ]
  • [ 111-86-4 ]
  • [ 64690-19-3 ]
Reference: [1] Synlett, 2000, # 1, p. 116 - 118
  • 8
  • [ 4783-86-2 ]
  • [ 142-95-0 ]
  • [ 64690-19-3 ]
Reference: [1] Doklady Chemistry, 1984, vol. 275, p. 97 - 100[2] Doklady Akademii Nauk SSSR, 1984, vol. 275, p. 385 - 387
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