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[ CAS No. 869557-43-7 ] {[proInfo.proName]}

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Chemical Structure| 869557-43-7
Chemical Structure| 869557-43-7
Structure of 869557-43-7 * Storage: {[proInfo.prStorage]}

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Product Details of [ 869557-43-7 ]

CAS No. :869557-43-7 MDL No. :MFCD03092924
Formula : C5H4BrFN2 Boiling Point : -
Linear Structure Formula :- InChI Key :KXSQMCRVUAALNE-UHFFFAOYSA-N
M.W : 191.00 Pubchem ID :16126434
Synonyms :
3-Bromo-5-fluoro-2-pyridinamine

Calculated chemistry of [ 869557-43-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 36.3
TPSA : 38.91 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.54 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.75
Log Po/w (XLOGP3) : 1.3
Log Po/w (WLOGP) : 1.99
Log Po/w (MLOGP) : 1.43
Log Po/w (SILICOS-IT) : 1.81
Consensus Log Po/w : 1.66

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -2.34
Solubility : 0.88 mg/ml ; 0.00461 mol/l
Class : Soluble
Log S (Ali) : -1.72
Solubility : 3.66 mg/ml ; 0.0192 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.8
Solubility : 0.303 mg/ml ; 0.00158 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.71

Safety of [ 869557-43-7 ]

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

Application In Synthesis of [ 869557-43-7 ]

* 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.

  • Downstream synthetic route of [ 869557-43-7 ]

[ 869557-43-7 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 869557-43-7 ]
  • potassium ferrocyanide [ No CAS ]
  • [ 801303-22-0 ]
  • 2
  • [ 869557-43-7 ]
  • potassium hexacyanoferrate(II) [ No CAS ]
  • [ 801303-22-0 ]
  • 3
  • [ 869557-43-7 ]
  • [ 557-21-1 ]
  • [ 801303-22-0 ]
YieldReaction ConditionsOperation in experiment
1,1'-bis-(diphenylphosphino)ferrocene; tris-(dibenzylideneacetone)dipalladium(0); In DMF (N,N-dimethyl-formamide); at 120℃; for 0.666667h;Microwave heating; In a microwave vessel was combined 3-bromo-5-fluoropyridin-2-amine (2.0 g, 0.0105 mmol), Zn (CN)2 mg), DPPF (25 mg), and 5 mL wet DMF. The solution was then purged with N2(g) prior to the addition of Pd2dba (20 mg). The reaction was heated at 120 C for 40 mins in a microwave reactor. Crude material was purified by flash silica column to yield 570 mg solid yellow product, MS (M+H) = 138, H NMR (300 MHz, DMSO-D6) 8 ppm 6.86 (s, 2 H) 7.98 (dd, J=8.29, 3.01 Hz, 1 H) 8.26 (d, J=3.01 Hz, 1 H).
  • 4
  • [ 869557-43-7 ]
  • copper(l) cyanide [ No CAS ]
  • [ 801303-22-0 ]
YieldReaction ConditionsOperation in experiment
0.59 g of copper(I) cyanide was added to a mixture of 1.04 g of the 2-amino-3-bromo-5-fluoropyridine and 20 ml of N-methyl-2-pyrrolidone, and the obtained mixture was stirred at 150C for 5 hours. Thereafter, 28% aqueous ammonia was added to the reaction mixture, and it was then extracted with ethyl acetate. The organic layer was washed with a saturated saline solution, and it was then dried over anhydrous sodium sulfate, followed by concentration under reduced pressure. The obtained residue was subjected to silica gel column chromatography, so as to obtain 0.52 g of 2-amino-3-cyano-5-fluoropyridine.2-amino-3-cyano-5-fluoropyridine [Show Image] 1H-NMR (CDCl3) delta: 5.10 (2H, br s), 7.45 (1H, dd, J = 7.4, 3.0 Hz), 8.16 (1H, d, J = 3.0 Hz).
  • 5
  • [ 869557-43-7 ]
  • potassiumhexacyanoferrate(II) trihydrate [ No CAS ]
  • [ 801303-22-0 ]
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