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[ CAS No. 872041-86-6 ] {[proInfo.proName]}

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Chemical Structure| 872041-86-6
Chemical Structure| 872041-86-6
Structure of 872041-86-6 * Storage: {[proInfo.prStorage]}

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Product Details of [ 872041-86-6 ]

CAS No. :872041-86-6 MDL No. :MFCD07368243
Formula : C5H5BFNO2 Boiling Point : -
Linear Structure Formula :- InChI Key :FVEDGBRHTGXPOK-UHFFFAOYSA-N
M.W : 140.91 Pubchem ID :44717403
Synonyms :

Calculated chemistry of [ 872041-86-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 4.0
Num. H-bond donors : 2.0
Molar Refractivity : 34.02
TPSA : 53.35 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -7.26 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : -0.14
Log Po/w (WLOGP) : -0.68
Log Po/w (MLOGP) : -0.93
Log Po/w (SILICOS-IT) : -0.72
Consensus Log Po/w : -0.49

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.0
Solubility : 14.0 mg/ml ; 0.0992 mol/l
Class : Very soluble
Log S (Ali) : -0.53
Solubility : 41.9 mg/ml ; 0.298 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.17
Solubility : 9.57 mg/ml ; 0.0679 mol/l
Class : Soluble

Medicinal Chemistry

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

Safety of [ 872041-86-6 ]

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 [ 872041-86-6 ]

* 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 [ 872041-86-6 ]

[ 872041-86-6 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 872041-86-6 ]
  • [ 4522-35-4 ]
  • C8H5FIN3 [ No CAS ]
YieldReaction ConditionsOperation in experiment
84.82% With pyridine; pyridine N-oxide; oxygen; copper diacetate; In dichloromethane; at 20℃; for 48h; To a mixture of compound 180(30000mg, 1 5Smmol) and 102(32762mg, 232mmol) in DCM (2OrnL). was added pyridine (367.02mg, 4.64mmol), Cu(OAc)2(561.83mg, 3.O9mmoi) and i oxidopyridin-i--iurn (442.21 mg, 4.6Smmol, 3.OOEq) in one portion at room temperature. The mixture was stirred at room temperature for 48 hours under 02 protected. LCMS showed thereaction was completed. The mixture was filtrated and the filtrate was concentrated in reduced pressure. The residue was dissolved in ethyl acetate (4OmL). The organic phase was washed with water (3OmLx2), saturated brine (3OmLxi), dried over anhydrous Na2SO4, filtered and concentrated in vacuum. The residue was purified by silica gel chromatography to afford product 206(380.00mg. yield: 84.82%).LCM: m/z, 2899M+H).
  • 2
  • [ 939979-43-8 ]
  • [ 872041-86-6 ]
  • 5-chloro-7-(5-fluoro-3-pyridyl)-3-methylpyrazolo[1,5-a]pyrimidine [ No CAS ]
YieldReaction ConditionsOperation in experiment
52.7% With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; caesium carbonate; In 1,4-dioxane; water; at 110.0℃; for 1.0h;Microwave irradiation; Sealed tube; 5,7-Dichloro-3-methyl-pyrazolo[l,5-a]pyrimidine (190 mg, 938.52 mupiiotaomicron, 1 eq), (5-fluoro-3- pyridyl)boronic acid (138.86 mg, 985.45 muiotaetaomicron, 1.05 eq), Pd(dppf)Cl2 (68.67 mg, 93.85 muiotaetaomicron, 0.1 eq) and Cs2C03 (611.58 mg, 1.88 mmol, 2 eq) were taken up into a microwave tube in 1,4-dioxane (3 mL) and H20 (1 mL). The sealed tube was heated at 110 C for 1 h under microwave. The mixture was concentrated and water (10 mL) was added. The mixture was extracted with EtOAc (20 mL x 3). The combined organic layers were dried over Na2S04, filtered and concentrated to yield a residue which was purified on silica gel column chromatography (from PE/EtOAc = 1/0 to 10/3, TLC: PE/EtOAc = 3/1, Rf = 0.50) to yield 5-chloro-7-(5-fluoro-3-pyridyl)-3-methyl- pyrazolo[l,5-a]pyrimidine (130 mg, 494.92 mupiiotaomicron, 52.7% yield, 100.0%) purity) as a yellow solid. NMR (400 MHz, CDC13) delta ppm 8.97 (s, 1H), 8.69 (d, J = 2.7 Hz, 1H), 8.38-8.31 (m, 1H), 8.04 (s, 1H), 6.92 (s, 1H), 2.40 (s, 3H); ES-LCMS m/z 263.0, 265.0 [M+H]+.
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