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[ CAS No. 942947-95-7 ] {[proInfo.proName]}

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Chemical Structure| 942947-95-7
Chemical Structure| 942947-95-7
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Product Details of [ 942947-95-7 ]

CAS No. :942947-95-7 MDL No. :MFCD11110693
Formula : C5H3BrClN3O2 Boiling Point : -
Linear Structure Formula :- InChI Key :BLGCPXIDEMLKMS-UHFFFAOYSA-N
M.W : 252.45 Pubchem ID :45480236
Synonyms :

Calculated chemistry of [ 942947-95-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 50.17
TPSA : 84.73 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.28 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.91
Log Po/w (XLOGP3) : 2.2
Log Po/w (WLOGP) : 2.52
Log Po/w (MLOGP) : 0.41
Log Po/w (SILICOS-IT) : 0.35
Consensus Log Po/w : 1.28

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.1
Solubility : 0.203 mg/ml ; 0.000803 mol/l
Class : Soluble
Log S (Ali) : -3.61
Solubility : 0.0615 mg/ml ; 0.000244 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.0
Solubility : 0.253 mg/ml ; 0.001 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 2.15

Safety of [ 942947-95-7 ]

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

Application In Synthesis of [ 942947-95-7 ]

* 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 [ 942947-95-7 ]

[ 942947-95-7 ] Synthesis Path-Upstream   1~3

  • 1
  • [ 6980-08-1 ]
  • [ 942947-95-7 ]
YieldReaction ConditionsOperation in experiment
99% With N-Bromosuccinimide In acetonitrile at 80℃; A solution of 4-chloro-3-nitropyridin-2-amine (2 g, 11.5 mmol) and N-bromosuccinimide (2.5 g, 13.8 mmol) in ACN (125 mL) was heated at 80 °C. After 1h, the reaction mixture was cooled was cooled to room temperature and volatiles were removed under reduced pressure. Purification (FCC, SiO2, 0-5percent EtOAc in DCM), afforded the title compound (2.9 g, 99percent). MS (ESI): mass calcd. for C5H3BrClN3O2, 250.9; m/z found, 251.8 [M+H]+.1H NMR (400 MHz, DMSO-d6) δ 8.42 (s, 1H), 7.37 (br s, 2H).
85% With N-Bromosuccinimide In acetonitrile at 80℃; for 1 h; 4-Chloro-3-nitropyridin-2-amine (0.1 0 g, 0.58 mmol) was dissolved in dryacetonitrile (20 ml). To the stirred solution was then added N-bromosuccinimide (0.124g, 0.70 mmol), and the reaction mixture was heated at 80 °C for 1 h. Volatiles wereremoved in vacuo and the residue purified by silica column chromatography (elution with25 dichloromethane) to provide the title compound as a pale brown powder (0.125 g, 85percent).1 H-NMR (500 MHz, DMSO-d6) 7.35 (s, 2H, NH2), 8.41 (s, 1 H, 6-H).
Reference: [1] Patent: WO2018/67786, 2018, A1, . Location in patent: Page/Page column 111
[2] Journal of Medicinal Chemistry, 2012, vol. 55, # 20, p. 8721 - 8734,14
[3] Journal of Medicinal Chemistry, 2012, vol. 55, # 20, p. 8721 - 8734
[4] Patent: WO2013/190320, 2013, A1, . Location in patent: Paragraph 00119
  • 2
  • [ 942947-94-6 ]
  • [ 942947-95-7 ]
Reference: [1] Patent: US2009/247507, 2009, A1, . Location in patent: Page/Page column 8
[2] Journal of Medicinal Chemistry, 2010, vol. 53, # 14, p. 5213 - 5228
[3] European Journal of Medicinal Chemistry, 2016, vol. 117, p. 19 - 32
  • 3
  • [ 19798-80-2 ]
  • [ 942947-95-7 ]
Reference: [1] Journal of Medicinal Chemistry, 2012, vol. 55, # 20, p. 8721 - 8734,14
[2] Journal of Medicinal Chemistry, 2012, vol. 55, # 20, p. 8721 - 8734
[3] Patent: WO2013/190320, 2013, A1,
[4] European Journal of Medicinal Chemistry, 2016, vol. 117, p. 19 - 32
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