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[ CAS No. 23833-99-0 ] {[proInfo.proName]}

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Chemical Structure| 23833-99-0
Chemical Structure| 23833-99-0
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Product Details of [ 23833-99-0 ]

CAS No. :23833-99-0 MDL No. :MFCD00457008
Formula : C9H5ClN2O2 Boiling Point : -
Linear Structure Formula :- InChI Key :AOATVJLAFLBGPZ-UHFFFAOYSA-N
M.W : 208.60 Pubchem ID :610440
Synonyms :

Calculated chemistry of [ 23833-99-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 14
Num. arom. heavy atoms : 10
Fraction Csp3 : 0.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 55.58
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) : -5.71 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.56
Log Po/w (XLOGP3) : 2.62
Log Po/w (WLOGP) : 2.8
Log Po/w (MLOGP) : 2.04
Log Po/w (SILICOS-IT) : 0.86
Consensus Log Po/w : 1.98

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.25
Solubility : 0.118 mg/ml ; 0.000567 mol/l
Class : Soluble
Log S (Ali) : -3.5
Solubility : 0.0655 mg/ml ; 0.000314 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.7
Solubility : 0.0412 mg/ml ; 0.000198 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.78

Safety of [ 23833-99-0 ]

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

Application In Synthesis of [ 23833-99-0 ]

* 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.

  • Upstream synthesis route of [ 23833-99-0 ]
  • Downstream synthetic route of [ 23833-99-0 ]

[ 23833-99-0 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 23833-99-0 ]
  • [ 81764-16-1 ]
YieldReaction ConditionsOperation in experiment
200 mg With iron; ammonium chloride In ethanol; water for 2 h; Reflux General procedure: To a solution of N-(4,4-difluorocyclohexyl)-8-nitroquinazolin-4-amine (90 mg, 0.292 mmol) in EtOH (2 mL) were added iron powder (163 mg, 2.92 mmol) and NH4Cl (127 mg, 2.33 mmol) and the reaction mixture was heated at reflux for 2 h.
Then the reaction mixture was filtered through celite.
The celite bed was washed with 10percent MeOH in CHCl3.
The filtrate was washed with a saturated aq. NaHCO3 solution and water.
The organic layer was separated, dried, filtered and concentrated to afford 70 mg of the title product. 1H NMR (300 MHz, DMSO d6): δ 8.38 (s, 1H), 7.64 (d, J=7.2 Hz, 1H), 7.35 (d, J=7.8 Hz, 1H), 7.19-7.14 (t, J=7.8 Hz, 1H), 6.87 (d, J=7.8 Hz, 1H), 5.71 (s, 2H), 4.38 (m, 1H), 2.09-1.97 (m, 6H), 1.73-1.69 (m, 2H); MS (m/z): 279.12 (M+H)+.The title compound was prepared following the procedure described in step-2, Intermediate-9 using 4-chloro-8-nitroquinoline (Intermediate-11, step-2, 250 mg, 1.20 mmol), NH4Cl (513 mg, 9.60 mmol) and iron powder (671 mg, 12.0 mmol) in EtOH (6 mL) and water (3 mL) to afford 200 mg of the title product. 1H NMR (400 MHz, CDCl3): δ 8.69 ((d, J=4.6 Hz, 1H), 7.55-7.53 (d, J=8.4 Hz, 1H), 7.48 (d, J=4.6 Hz, 1H), 7.46-7.42 (t, J=7.6 Hz, 1H), 7.00-6.98 (d, J=7.6 Hz, 1H), 5.06 (br s, 2H); MS [M+H]+: 179.25.
Reference: [1] Dalton Transactions, 2012, vol. 41, # 38, p. 11776 - 11782
[2] Journal of the American Chemical Society, 1947, vol. 69, p. 303,306
[3] Journal of the American Chemical Society, 1946, vol. 68, p. 1524,1526
[4] Patent: US2013/210844, 2013, A1, . Location in patent: Paragraph 0322; 0517; 0518
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