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[ CAS No. 443882-99-3 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 443882-99-3
Chemical Structure| 443882-99-3
Structure of 443882-99-3 * Storage: {[proInfo.prStorage]}

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Product Details of [ 443882-99-3 ]

CAS No. :443882-99-3 MDL No. :MFCD06809827
Formula : C13H9ClFNO3 Boiling Point : No data available
Linear Structure Formula :- InChI Key :SFTHVDYRPHJAND-UHFFFAOYSA-N
M.W : 281.67 Pubchem ID :7059269
Synonyms :

Calculated chemistry of [ 443882-99-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 19
Num. arom. heavy atoms : 12
Fraction Csp3 : 0.08
Num. rotatable bonds : 4
Num. H-bond acceptors : 4.0
Num. H-bond donors : 0.0
Molar Refractivity : 71.21
TPSA : 55.05 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : Yes
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.22 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.3
Log Po/w (XLOGP3) : 3.94
Log Po/w (WLOGP) : 4.23
Log Po/w (MLOGP) : 3.9
Log Po/w (SILICOS-IT) : 2.24
Consensus Log Po/w : 3.32

Druglikeness

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

Water Solubility

Log S (ESOL) : -4.27
Solubility : 0.0151 mg/ml ; 0.0000535 mol/l
Class : Moderately soluble
Log S (Ali) : -4.8
Solubility : 0.00451 mg/ml ; 0.000016 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -5.33
Solubility : 0.00131 mg/ml ; 0.00000466 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.19

Safety of [ 443882-99-3 ]

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

Application In Synthesis of [ 443882-99-3 ]

* 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 [ 443882-99-3 ]

[ 443882-99-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 443882-99-3 ]
  • [ 98556-31-1 ]
  • [ 231278-20-9 ]
YieldReaction ConditionsOperation in experiment
Example 6: N-r3-Chloro-4-(3-Fluorobenzyloxy)-Phenyll-6-Iodoquinazolin-4-amine preparation (one-pot process)[00088] 30.0 g of "Intermediate-A" (compound of Formula A), 17.8 g of iron powder (70 mesh), 51.3 g of ammonium chloride, 432 ml of ethanol and 108 ml of water were refluxed for 5 hours in IL reactor equipped with mechanical stirrer and condenser. The reaction mixture was then cooled to 20-250C and separated from insoluble iron oxide by vacuum filtration. The filtered solids were washed with ethanol (4 x 100 ml). The resulting filtrate was evaporated from reactor under reduced pressure to resulting in a wet orange residue. The residue was dissolved in 350 ml of dichloromethane and 300 ml water. The separated organic phase was washed with water (2 x 300 ml). The obtained organic solution was concentrated to about 150 ml followed by addition of 300 ml iso- propanol. The mixture was concentrated to 300 ml followed by addition 150 ml iso- propanol. The resulting mixture was concentrated to 300 ml. Then iso-propanol was added to obtain a final volume of about 570 ml (purity determined by HPLC: 98.5%).[00089] 23.8 g of <strong>[98556-31-1]4-chloro-6-iodoquinazoline</strong> were added to the organic solution, heated to reflux, stirred for 30 minutes and then cooled to 20-250C. The slurry was filtered and washed with 110 ml iso-propanol to obtain 53.5 g of wet crude product. Then it was triturated in 830 ml of boiling acetone for an hour, cooled and filtered. The product was triturated twice again each time in 655 ml of boiling acetone for an hour, cooled and filtered. Finally it was dried at 250C in vacuum oven to afford 32.2 g of "Intermediate-C" (Yield: 60%, Purity: 92.62%).
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