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[ CAS No. 24100-18-3 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 24100-18-3
Chemical Structure| 24100-18-3
Structure of 24100-18-3 * Storage: {[proInfo.prStorage]}

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Product Details of [ 24100-18-3 ]

CAS No. :24100-18-3 MDL No. :MFCD01570896
Formula : C6H6BrNO Boiling Point : No data available
Linear Structure Formula :- InChI Key :PDOWLYNSFYZIQX-UHFFFAOYSA-N
M.W : 188.02 Pubchem ID :90364
Synonyms :

Calculated chemistry of [ 24100-18-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.17
Num. rotatable bonds : 1
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 38.43
TPSA : 22.12 ?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) : -6.49 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.94
Log Po/w (XLOGP3) : 1.35
Log Po/w (WLOGP) : 1.85
Log Po/w (MLOGP) : 0.92
Log Po/w (SILICOS-IT) : 2.04
Consensus Log Po/w : 1.62

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -2.28
Solubility : 0.979 mg/ml ; 0.00521 mol/l
Class : Soluble
Log S (Ali) : -1.42
Solubility : 7.2 mg/ml ; 0.0383 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -3.01
Solubility : 0.185 mg/ml ; 0.000986 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.87

Safety of [ 24100-18-3 ]

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 [ 24100-18-3 ]

* 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.

  • Upstream synthesis route of [ 24100-18-3 ]
  • Downstream synthetic route of [ 24100-18-3 ]

[ 24100-18-3 ] Synthesis Path-Upstream   1~2

  • 1
  • [ 24100-18-3 ]
  • [ 76066-07-4 ]
YieldReaction ConditionsOperation in experiment
64% at 0 - 55℃; for 1.5 h; 2-Amino-5.6-dimethoxypyridine(a) 2-Bromo-3 -methoxy-6-nitropyridine2-Bromo-3-methoxypyridine (4.45 g, 23.7 mmol) was added to a mixture of fuming HNO3 and concentrated H2SO4 (1:1, 18 mL) at O0C. The mixture was stirred at 55°C for 1.5 h and then poured into ice water (150 mL). The precipitate formed was the pure product, which was used without further purification. Yield: 3.54 g (64percent) of slightly yellow solid.1HNMR (DMSOd6, 400 MHz) δ 8.41 (d, IH), 7.80 (d, IH), 4.06 (s, 3H).
64% With sulfuric acid; nitric acid In water at 0 - 55℃; for 1.5 h; 2-Bromo-3-methoxypyridine (4.45 g, 23.7 mmol) was added to a mixture of fuming HNO3 and concentrated H2SO4 (1:1, 18 mL) at 0 0C. The mixture was stirred at 55 0C for 1.5 h and then poured into ice water (150 mL). The precipitate formed was filtered off, washed with water (3x100 mL) and dried in vacuo to give 3.54 g (64percent) of slightly yellow solid, which was essentially pure product. 1HNMR (DMSO-de, 400 MHz) δ 8.41 (d, IH), 7.80 (d, IH), 4.06 (s, 3H).
60 mg at 55℃; for 3 h; To a solution of 2-bromo-3-methoxypyridine (0.1 g) in conc. sulfuric acid (2 mL) wasadded nitric acid (0.1 g). The mixture was stirred at 55°C for 3 hours. After cooling, the mixturewas poured into water (10 mL). The mixture was filtered. The solid was washed with water,and then redissolved in DCM. The solution was dried over Na2SO4 and concentrated in vacuo to afford 2-bromo-3-methoxy-6-nitropyridine (60 mg). MS(ES) m/z 233 (MH).
Reference: [1] Journal of Medicinal Chemistry, 2009, vol. 52, # 3, p. 637 - 645
[2] Tetrahedron, 1986, vol. 42, # 5, p. 1475 - 1485
[3] Pharmazie, 2000, vol. 55, # 12, p. 907 - 912
[4] Journal of Medicinal Chemistry, 1981, vol. 24, # 1, p. 39 - 42
[5] Patent: WO2007/51981, 2007, A1, . Location in patent: Page/Page column 56
[6] Patent: WO2007/51982, 2007, A1, . Location in patent: Page/Page column 48
[7] Australian Journal of Chemistry, 1981, vol. 34, # 4, p. 927 - 932
[8] Patent: EP2022792, 2009, A1, . Location in patent: Page/Page column 10; 28
[9] Patent: EP2042501, 2009, A1, . Location in patent: Page/Page column 2; 8-9; 15; 24-25
[10] Patent: EP2098523, 2009, A1, . Location in patent: Page/Page column 10
[11] Patent: EP2216051, 2010, A1,
[12] Patent: EP2216052, 2010, A1,
[13] Patent: EP2213671, 2010, A1, . Location in patent: Page/Page column 9; 24
[14] Patent: EP2213672, 2010, A1, . Location in patent: Page/Page column 15; 27
[15] Patent: WO2015/181186, 2015, A1, . Location in patent: Page/Page column 131
  • 2
  • [ 24100-18-3 ]
  • [ 7664-93-9 ]
  • [ 76066-07-4 ]
Reference: [1] Patent: US5929094, 1999, A,
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