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[ CAS No. 1150271-53-6 ]

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Chemical Structure| 1150271-53-6
Chemical Structure| 1150271-53-6
Structure of 1150271-53-6 * Storage: {[proInfo.prStorage]}
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Product Details of [ 1150271-53-6 ]

CAS No. :1150271-53-6 MDL No. :MFCD09998360
Formula : C20H26BNO2 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W :323.24 Pubchem ID :-
Synonyms :

Calculated chemistry of [ 1150271-53-6 ]

Physicochemical Properties

Num. heavy atoms : 24
Num. arom. heavy atoms : 12
Fraction Csp3 : 0.4
Num. rotatable bonds : 5
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 99.98
TPSA : 30.49 Ų

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : Yes
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : Yes
CYP3A4 inhibitor : Yes
Log Kp (skin permeation) : -5.6 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 3.77
Log Po/w (WLOGP) : 2.97
Log Po/w (MLOGP) : 2.59
Log Po/w (SILICOS-IT) : 3.42
Consensus Log Po/w : 2.55

Druglikeness

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

Water Solubility

Log S (ESOL) : -4.26
Solubility : 0.0178 mg/ml ; 0.0000551 mol/l
Class : Moderately soluble
Log S (Ali) : -4.1
Solubility : 0.0255 mg/ml ; 0.0000788 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -7.35
Solubility : 0.0000144 mg/ml ; 0.0000000445 mol/l
Class : Poorly soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 3.31

Safety of [ 1150271-53-6 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P330-P363-P501 UN#:
Hazard Statements:H302-H312-H332 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 1150271-53-6 ]

* 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 [ 1150271-53-6 ]

[ 1150271-53-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1150271-53-6 ]
  • [ 2244903-56-6 ]
  • [ 2244905-04-0 ]
YieldReaction ConditionsOperation in experiment
63 mg With tetrakis(triphenylphosphine) palladium(0); potassium carbonate In 1,4-dioxane; water at 110℃; 365 Example 365 N-[1-(5-{2-[(benzylamino)methyl]phenyl}thiophen-2-yl)ethyl]-6,7-dimethoxy-2- methylquinazolin-4-amine A mixture of N-[1 -(5-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazolin-4-amine (prepared as described in example 209; 100 mg, 0.24 mmol), 2-(N- benzylaminomethyl)phenylboronic acid, pinacol ester (commercially available; 80.8 mg, 0.24 mmol), potassium carbonate (135.4 mg, 0.98 mmol) and tetrakis(triphenylphosphin) palladium(O) (28.3 mg, 0.025 mmol) in dioxane (2.5 mL) and water (0.5 mL) was stirred at 1 10°C overnight. The reaction mixture was evaporated and the crude product was purified via HPLC to yield 48% of the title compound (63 mg). 1H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.14 (d, 1H), 7.65 (s, 1H), 7.54 (d, 1H), 7.34-7.22 (m, 7H), 7.22-7.14 (m, 1H), 7.1 1 (d, 1H), 7.06-7.03 (m, 2H), 5.96 (t, 1H), 3.86 (d, 6H), 3.73-3.61 (m, 4H), 2.54-2.52 (m, 1H), 2.44-2.40 (m, 3H), 1.71 (d, 3H). LC-MS (method 7): m/z: [M+H]+ = 525.2, Rt = 0.66 min.
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