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[ CAS No. 426463-09-4 ] {[proInfo.proName]}

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Chemical Structure| 426463-09-4
Chemical Structure| 426463-09-4
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Product Details of [ 426463-09-4 ]

CAS No. :426463-09-4 MDL No. :MFCD04038465
Formula : C5H4ClIN2 Boiling Point : -
Linear Structure Formula :- InChI Key :CIKQIWYGYUILOL-UHFFFAOYSA-N
M.W : 254.46 Pubchem ID :1514296
Synonyms :

Calculated chemistry of [ 426463-09-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 46.37
TPSA : 38.91 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.59 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.56
Log Po/w (XLOGP3) : 1.78
Log Po/w (WLOGP) : 1.93
Log Po/w (MLOGP) : 1.36
Log Po/w (SILICOS-IT) : 2.32
Consensus Log Po/w : 1.79

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.03
Solubility : 0.236 mg/ml ; 0.000928 mol/l
Class : Soluble
Log S (Ali) : -2.22
Solubility : 1.55 mg/ml ; 0.00609 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.24
Solubility : 0.148 mg/ml ; 0.000581 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 2.34

Safety of [ 426463-09-4 ]

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

Application In Synthesis of [ 426463-09-4 ]

* 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 [ 426463-09-4 ]
  • Downstream synthetic route of [ 426463-09-4 ]

[ 426463-09-4 ] Synthesis Path-Upstream   1~5

  • 1
  • [ 426463-05-0 ]
  • [ 426463-09-4 ]
YieldReaction ConditionsOperation in experiment
92% With hydrogenchloride; iron In ethanol; hexane; water; ethyl acetate 5-Iodo-3-amino-2-chloropyridine
5-iodo-3-nitro-2-chloropyridine (230 mg, 0.809 mmol), ethanol (1 mL), water (6 drops), and concentrated HCl (0.020 mL) were stirred at room temperature for 10 min.
Iron (500 mg, 8.95 mmol) was then added in small portions and the reaction round bottom flask was placed into a 100° C. oil bath for 20 min.
The iron was removed by filtration, washed with ethanol, then the combined ethanol layers were concentrated under reduced pressure.
The crude residue was purified by flash chromatography using 9:1 hexane: ethyl acetate to give 5-iodo-3-amino-2-chloropyridine (190 mg, 92percent) as a colorless solid.
mp 129° C.; 1H NMR (CDCl3) δ (ppm) 4.15 (br s, 2H), 7.34 (d, J=2.0 Hz, 1H), 7.96 (d, J=2.0 Hz, 1H); 13C NMR (CDCl3) δ (ppm) 91.41, 129.67, 136.31, 140.77, 143.90.
Analytical Calculated for C5H4N2lCl: C, 23.60; H, 1.58; N, 11.01; Found: C, 23-66; H, 1.52; N, 10.98.
Reference: [1] Journal of Organic Chemistry, 2011, vol. 76, # 23, p. 9841 - 9844
[2] Journal of Medicinal Chemistry, 2002, vol. 45, # 21, p. 4755 - 4761
[3] Patent: US6538010, 2003, B1,
[4] Bioorganic & Medicinal Chemistry Letters, 2003, vol. 13, # 3, p. 525 - 528
  • 2
  • [ 4214-75-9 ]
  • [ 426463-09-4 ]
Reference: [1] Journal of Medicinal Chemistry, 2002, vol. 45, # 21, p. 4755 - 4761
  • 3
  • [ 25391-57-5 ]
  • [ 426463-09-4 ]
Reference: [1] Journal of Medicinal Chemistry, 2002, vol. 45, # 21, p. 4755 - 4761
  • 4
  • [ 6332-56-5 ]
  • [ 426463-09-4 ]
Reference: [1] Bioorganic & Medicinal Chemistry Letters, 2003, vol. 13, # 3, p. 525 - 528
  • 5
  • [ 25391-59-7 ]
  • [ 426463-09-4 ]
Reference: [1] Bioorganic & Medicinal Chemistry Letters, 2003, vol. 13, # 3, p. 525 - 528
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