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[ CAS No. 186593-42-0 ] {[proInfo.proName]}

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Chemical Structure| 186593-42-0
Chemical Structure| 186593-42-0
Structure of 186593-42-0 * Storage: {[proInfo.prStorage]}

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Product Details of [ 186593-42-0 ]

CAS No. :186593-42-0 MDL No. :MFCD08688606
Formula : C6H5BrN2O2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :QWAOQTGMEGSRLN-UHFFFAOYSA-N
M.W : 217.02 Pubchem ID :18458822
Synonyms :

Calculated chemistry of [ 186593-42-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.17
Num. rotatable bonds : 1
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 45.73
TPSA : 58.71 ?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) : -6.37 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.51
Log Po/w (XLOGP3) : 1.77
Log Po/w (WLOGP) : 2.06
Log Po/w (MLOGP) : 1.2
Log Po/w (SILICOS-IT) : 0.34
Consensus Log Po/w : 1.38

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.64
Solubility : 0.499 mg/ml ; 0.0023 mol/l
Class : Soluble
Log S (Ali) : -2.62
Solubility : 0.52 mg/ml ; 0.00239 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.65
Solubility : 0.484 mg/ml ; 0.00223 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.01

Safety of [ 186593-42-0 ]

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

Application In Synthesis of [ 186593-42-0 ]

* 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 [ 186593-42-0 ]

[ 186593-42-0 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 186593-42-0 ]
  • [ 66521-66-2 ]
  • 2-methyl-3-(4-pyridin-3-yl)pyrimidin-2-ylamino-5-nitropyridine [ No CAS ]
YieldReaction ConditionsOperation in experiment
50% With caesium carbonate; 4,5-bis(diphenylphos4,5-bis(diphenylphosphino)-9,9-dimethylxanthenephino)-9,9-dimethylxanthene;tris-(dibenzylideneacetone)dipalladium(0); In toluene; at 90℃; for 16h;Inert atmosphere; EXAMPLE 1:4-((4-ethylpiperazin-l-yl)methyl)-N-(6-methyl-5-(4-(pyridin-3-yl)pyrimidin-2- ylamino)pyridin-3-yl)benzamide(a) (2-Methyl-5-nitro-pyridin-3-yl)-(4-pyridin-3-yl-pyrimidin-2-yl)-amine[0121] To a mixture of 3-bromo-2-methyl-5-nitro-pyridine (380mg, 1.75mmol) and 4-pyridin-3-yl-pyrimidin-2-ylamine (250mg, 1.45mmol) in dry toluene (2OmL) were added Cs2CO3 (710mg, 2.18mmol), Pd2(dba)3 (26mg, 0.028mmol) and Xantphos (50mg, 0.086mmol). The mixture was evacuated and purged with N2 (3 cycles), heated to 9O0C under N2 for 16h. After completion (monitored by TLC), the reaction mixture was cooled to rt, diluted with EtOAc and filtered. The filtrate was concentrated under reduced pressure and the residue was purified by column chromatography (SiO2) using CH2Cl2-MeOH (98:2) to afford product (225mg, 50percent). 1H NMR (200 MHz, CDCl3): delta 2.76 (s, 3H), 7.23 (m, IH), 7.38 (d, J= 6.0 Hz, IH), 7.51 (m, IH), 8.51 (m, IH), 8.63 ( d, J= 6.0 Hz, IH), 8.77 (m, IH), 9.04 (d, J= 2.0 Hz, IH), 9.28 (d, J= 2.0 Hz, IH), 9.77 (d, J= 2.0 Hz, IH); Mass [M+H]+: 309.
  • 2
  • [ 186593-42-0 ]
  • [ 1621225-24-8 ]
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