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[ CAS No. 1036991-24-8 ] {[proInfo.proName]}

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Chemical Structure| 1036991-24-8
Chemical Structure| 1036991-24-8
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Product Details of [ 1036991-24-8 ]

CAS No. :1036991-24-8 MDL No. :MFCD11975406
Formula : C13H21BN2O2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :KSAMKARQFVLMFC-UHFFFAOYSA-N
M.W : 248.13 Pubchem ID :51072189
Synonyms :

Calculated chemistry of [ 1036991-24-8 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 18
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.62
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 74.92
TPSA : 34.59 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : Yes
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.19 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 2.29
Log Po/w (WLOGP) : 1.45
Log Po/w (MLOGP) : 0.96
Log Po/w (SILICOS-IT) : 0.92
Consensus Log Po/w : 1.12

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.94
Solubility : 0.288 mg/ml ; 0.00116 mol/l
Class : Soluble
Log S (Ali) : -2.65
Solubility : 0.55 mg/ml ; 0.00222 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.74
Solubility : 0.0452 mg/ml ; 0.000182 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 3.13

Safety of [ 1036991-24-8 ]

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 [ 1036991-24-8 ]

* 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 [ 1036991-24-8 ]

[ 1036991-24-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 26163-07-5 ]
  • [ 73183-34-3 ]
  • [ 1036991-24-8 ]
YieldReaction ConditionsOperation in experiment
76% With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium acetate; In 1,4-dioxane; at 100℃; for 12h;Inert atmosphere; To a solution of 5-bromo-2-(NN-dimethylamino)pyridine (8.5 g, 42.3 mmol) and 4,4,4',4',5,5,5',5'-octamethyl-2,2'-bi(1,3,2-dioxaborolane) (12.9 g, 50.7 mmol) in dioxane (10 mL) was added KOAc (8.3 g, 84.6 mmol) and Pd(dppf)Cl2 (1.55 g, 2.1 mmol) at 25 C under N2. The mixture was heated to 100 C and stirred at this temperature for 12 hours. LCMS showed that the reaction was complete. The mixture was filtered and concentrated under reduced pressure to give a residue which was purified by silica gel column chromatography (petroleum ether / ethyl acetate=50/1 to 3/1) to give 2-(2-(N,N-dimethylamino)pyrid-5-yl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (8 g, 32.2 mmol, 76% yield) as a yellow solid 1H NMR 400 MHz CDCl3 = 8.53 (s, 1H), 7.75-7.78 (d, 1H), 6.43-6.45 (d, 1H), 3.09 (s, 6H), 1.22-1.30 (m, 12H). ESI-MS (m/z): 249.2 (M+H)+
With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; potassium acetate; In 1,4-dioxane; at 20℃;Inert atmosphere; PdCI2(dppf)-CH2Cl2 adduct (81 mg, 0.099 mmol) was added to a solution of 4,4,4',4',5,5,5',5'-octamethyl-2,2'-bi(1 ,3,2-dioxaborolane) (379 mg, 1 .492 mmol), 5-bromo- N,N-dimethylpyridin-2-amine (200 mg, 0.995 mmol) and potassium acetate (293 mg, 2.98 mmol) in 1 ,4-dioxane (40 mL) at room temperature under an atmosphere of nitrogen. The resulting solution was stirred at 100 C for 12 hr. The system was filtered and the filtrate was concentrated to afford crude product.which was used for the next step. LCMS: [M+H] 249.1 .
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