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[ CAS No. 381233-96-1 ] {[proInfo.proName]}

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Chemical Structure| 381233-96-1
Chemical Structure| 381233-96-1
Structure of 381233-96-1 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 381233-96-1 ]

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Product Citations

Product Details of [ 381233-96-1 ]

CAS No. :381233-96-1 MDL No. :MFCD06659000
Formula : C5H4BrIN2 Boiling Point : -
Linear Structure Formula :- InChI Key :XPERZSKJGNUSHI-UHFFFAOYSA-N
M.W : 298.91 Pubchem ID :1516508
Synonyms :

Calculated chemistry of [ 381233-96-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 49.06
TPSA : 38.91 ?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) : -6.81 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.78
Log Po/w (XLOGP3) : 1.85
Log Po/w (WLOGP) : 2.04
Log Po/w (MLOGP) : 1.92
Log Po/w (SILICOS-IT) : 2.35
Consensus Log Po/w : 1.99

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.35
Solubility : 0.133 mg/ml ; 0.000445 mol/l
Class : Soluble
Log S (Ali) : -2.29
Solubility : 1.54 mg/ml ; 0.00515 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.46
Solubility : 0.104 mg/ml ; 0.000348 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 2.14

Safety of [ 381233-96-1 ]

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 [ 381233-96-1 ]

* 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 [ 381233-96-1 ]

[ 381233-96-1 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 381233-96-1 ]
  • [ 1217501-27-3 ]
  • 5-bromo-3-(3-methyl-1H-pyrazol-5-yl)pyridin-2-amine [ No CAS ]
  • 9-bromo-2-methylpyrazolo[1,5-c]pyrido[3,2-e]pyrimidin-5-ol [ No CAS ]
YieldReaction ConditionsOperation in experiment
With tetrakis(triphenylphosphine) palladium(0); caesium carbonate; In 1,2-dimethoxyethane; water; at 130 - 150℃; for 4.5h;Microwave irradiation; Pd(PPh3)4 (190.0 mg, 0.17 mmol) was added to suspension of 5-bromo-3-iodopyridin-2-amine (500.0 mg, 1.67 mmol), <strong>[1217501-27-3](1-(tert-butoxycarbonyl)-3-methyl-1H-pyrazol-5-yl)boronic acid</strong> (755.0 mg, 3.34 mmol), Cs2CO3 (1600.0 mg, 5.01 mmol), H2O (3.0 mL) and DME (12.0 mL). The reaction mixture was allowed to react in microwave under conditions of 100 W and 130 C. for 2 hours and 30 minutes, followed by 100 W and 150 C. for 2 hours and then cooled to room temperature. Water was added to the reaction mixture, and it was extracted 2 times with EtOAc. The organic layer was dried over anhydrous Na2SO4, filtered and then concentrated under reduced pressure. The residue was purified by column chromatography (MeOH:DCM=1:40) on silica. The fractions containing the product were collected and evaporated to obtain brown solid compound which is the mixture of 5-bromo-3-(3-methyl-1H-pyrazol-5-yl)pyridin-2-amine and 9-bromo-2-methylpyrazolo[1,5-c]pyrido[3,2-e]pyrimidin-5-ol (78.0 mg).
  • 2
  • [ 381233-96-1 ]
  • [ 1210838-82-6 ]
  • 3
  • [ 381233-96-1 ]
  • [ 1049730-42-8 ]
  • 5-bromo-3-[1-(2,2,2-trifluoro-ethyl)-1H-pyrazol-4-yl]pyridin-2-ylamine [ No CAS ]
YieldReaction ConditionsOperation in experiment
58% With bis-triphenylphosphine-palladium(II) chloride; sodium carbonate; In ethanol; toluene; at 90℃; for 3h; Intermediate C1 (2881) 5-Bromo-3-[1-(2,2,2-trifluoro-ethyl)-1H-pyrazol-4-yl]-pyridin-2-ylamine (2882) (2883) Sodium carbonate (2.76 ml of a 2M solution, 5.52 mmol) was added to a mixture of 5-bromo- 3-iodopyridin-2-amine (0.55 g, 1.84 mmol), 4-(4,4,5,5-tetramethyl-1 ,3,2-dioxoborolan-2-yl)-1- (2,2,2-trifluoroethyl)-1 H-pyrazole (0.61 g, 2.21 mmol) (Intermediate D1) and Pd(PPh3)2CI2 (0.065 g, 0.092 mmol) in toluene (7 ml) and ethanol (3.5 ml). The mixture was heated at 90C. After 3h the reaction was complete by LCMS. The reaction mixture was diluted with EtOAc and washed with brine. The organic extract was dried over MgS04 and the crude product absorbed on silica. Chromatography on silica, eluting with EtOAc, gave the product as a grey solid (0.36 g, 58 %); (2884) LCMS: Rt 1.00 mins; MS m/z 321.3 [M+H]+ ; Method 2minLC_v003 (2885) 1H NMR (400MHz, CDCI3) 8.15 (1 H, br s), 7.82 (1 H, s), 7.78 (1 H, s), 7.55 (1 H, s), 4.7 (2H, m)
  • 4
  • [ 381233-96-1 ]
  • [ 871329-84-9 ]
  • 3-(2-amino-5-(3,5-difluoro-4-hydroxyphenyl)pyridin-3-yl)-5-fluorobenzoic acid [ No CAS ]
  • 5
  • [ 381233-96-1 ]
  • [ 871329-84-9 ]
  • C12H8BrFN2O2 [ No CAS ]
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Technical Information

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[2,3'-Bipyridin]-6'(1'H)-one

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3-Bromo-5-(2-pyridyl)-1-phenyl-1,2-dihydropyridin-2-one

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5-Bromopyridin-2-amine

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(4-Chlorophenyl)boronic acid

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