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[ CAS No. 928839-62-7 ] {[proInfo.proName]}

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Chemical Structure| 928839-62-7
Chemical Structure| 928839-62-7
Structure of 928839-62-7 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 928839-62-7 ]

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Product Details of [ 928839-62-7 ]

CAS No. :928839-62-7 MDL No. :MFCD19689072
Formula : C10H6BrNO2 Boiling Point : -
Linear Structure Formula :- InChI Key :SMDUUZMMJKRMDS-UHFFFAOYSA-N
M.W : 252.06 Pubchem ID :59292860
Synonyms :

Calculated chemistry of [ 928839-62-7 ]      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 : 1.0
Molar Refractivity : 56.4
TPSA : 50.19 ?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) : -6.17 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.53
Log Po/w (XLOGP3) : 2.35
Log Po/w (WLOGP) : 2.7
Log Po/w (MLOGP) : 2.04
Log Po/w (SILICOS-IT) : 2.47
Consensus Log Po/w : 2.22

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 0.0
Bioavailability Score : 0.56

Water Solubility

Log S (ESOL) : -3.35
Solubility : 0.114 mg/ml ; 0.000451 mol/l
Class : Soluble
Log S (Ali) : -3.04
Solubility : 0.228 mg/ml ; 0.000904 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.93
Solubility : 0.0295 mg/ml ; 0.000117 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 1.38

Safety of [ 928839-62-7 ]

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 [ 928839-62-7 ]

* 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 [ 928839-62-7 ]

[ 928839-62-7 ] Synthesis Path-Upstream   1~6

  • 1
  • [ 74316-55-5 ]
  • [ 928839-62-7 ]
YieldReaction ConditionsOperation in experiment
62% With chromium(VI) oxide; sulfuric acid In water at 90℃; for 2 h; Step 2: S-bromoquinoline-S-carboxylic acidA solution (0.1 M) of 5-bromo-8-methylquinoline (from Step 1) in H2SOzrH2O (3:2) was treated with Cr?3 (10 eq.) at 900C. The reaction mixture was heated at 900C for 2 h. Then, the mixture was poured into ice and the precipitate was filtered affording (62percent) the title compound as an orange solid; MS (ES+) m/z 252, 254 (M+H)+.
Reference: [1] Bioorganic and Medicinal Chemistry, 2010, vol. 18, # 8, p. 2836 - 2848
[2] Patent: WO2007/28789, 2007, A1, . Location in patent: Page/Page column 34
[3] Patent: WO2013/96194, 2013, A1,
[4] Patent: WO2015/84842, 2015, A1, . Location in patent: Paragraph 0089
[5] Patent: WO2009/141386, 2009, A1, . Location in patent: Page/Page column 162; 163
  • 2
  • [ 885267-41-4 ]
  • [ 928839-62-7 ]
Reference: [1] Patent: WO2013/96194, 2013, A1, . Location in patent: Page/Page column 32
  • 3
  • [ 611-32-5 ]
  • [ 928839-62-7 ]
Reference: [1] Patent: WO2013/96194, 2013, A1,
[2] Patent: WO2009/141386, 2009, A1,
  • 4
  • [ 1309959-33-8 ]
  • [ 928839-62-7 ]
Reference: [1] Patent: WO2013/96194, 2013, A1,
  • 5
  • [ 20776-50-5 ]
  • [ 56-81-5 ]
  • [ 928839-62-7 ]
Reference: [1] Journal of Organic Chemistry, 2013, vol. 78, # 17, p. 8217 - 8231
  • 6
  • [ 928839-62-7 ]
  • [ 74-88-4 ]
  • [ 1445781-45-2 ]
YieldReaction ConditionsOperation in experiment
20.5 g With potassium carbonate In N,N-dimethyl-formamide at 45℃; for 36 h; [0090] (b) K2C03 (61.3 g, 444.0 mmol) and methyl iodide (63.1 g, 444.0 mmol) were added to a stirred suspension of 5-bromoquinoline-8-carboxylic acid (28.0 g, 111.0 mmol) in DMF (250 mL) at r.t. The reaction mixture was heated at 45 0 C for 36 h, cooled to r.t, filtered the solids, washed with ethyl acetate (100 mL). The filtrate was diluted with water, extracted with ethyl acetate (3 x 300 mL) and washed with water (3 x 100 mL). The ethyl acetate layer was dried (Na2S04), filtered and concentrated under reduced pressure. The residue was purified by flash column chromatography on silica gel, eluting with ethyl acetate in hexanes (0-20percent) to afford methyl-5-bromoquinoline-8-carboxylate as a cream color solid (20.5 g, 70 percent for 2 steps). 1H NMR (400 MHz, CDC13) δ 9.07 (dd, J = 4.3, 1.5 Hz, 1 H), 8.60 (dd, J = 8.7, 1.6 Hz, 1 H), 7.88 (s, 2 H), 7.58 (dd, J = 8.6, 4.0 Hz, 1 H), 4.05 (s, 3 H)
Reference: [1] Patent: WO2013/96194, 2013, A1, . Location in patent: Page/Page column 33
[2] Patent: WO2015/84842, 2015, A1, . Location in patent: Paragraph 0090
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