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[ CAS No. 211943-13-4 ]

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Cat. No.: {[proInfo.prAm]}
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Chemical Structure| 211943-13-4
Chemical Structure| 211943-13-4
Structure of 211943-13-4 * Storage: {[proInfo.prStorage]}
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Product Details of [ 211943-13-4 ]

CAS No. :211943-13-4 MDL No. :MFCD02093928
Formula : C6H4BrN5 Boiling Point : -
Linear Structure Formula :- InChI Key :XJGDASCALCDOQH-UHFFFAOYSA-N
M.W :226.03 g/mol Pubchem ID :4173761
Synonyms :

Calculated chemistry of [ 211943-13-4 ]

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 11
Fraction Csp3 : 0.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 4.0
Num. H-bond donors : 1.0
Molar Refractivity : 45.11
TPSA : 67.35 Ų

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -7.09 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.84
Log Po/w (XLOGP3) : 0.83
Log Po/w (WLOGP) : 1.02
Log Po/w (MLOGP) : 0.99
Log Po/w (SILICOS-IT) : 1.82
Consensus Log Po/w : 1.1

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 0.0
Bioavailability Score : 0.85

Water Solubility

Log S (ESOL) : -2.38
Solubility : 0.95 mg/ml ; 0.0042 mol/l
Class : Soluble
Log S (Ali) : -1.83
Solubility : 3.37 mg/ml ; 0.0149 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -3.5
Solubility : 0.0723 mg/ml ; 0.00032 mol/l
Class : Soluble

Medicinal Chemistry

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

Safety of [ 211943-13-4 ]

Signal Word:Danger Class:4.1
Precautionary Statements:P240-P210-P241-P264-P280-P302+P352-P370+P378-P337+P313-P305+P351+P338-P362+P364-P332+P313 UN#:1325
Hazard Statements:H315-H319-H228 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 211943-13-4 ]

* 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 [ 211943-13-4 ]

[ 211943-13-4 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 1620828-90-1 ]
  • [ 211943-13-4 ]
  • [ 1620827-68-0 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: caesium carbonate; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2 / tetrahydrofuran; water / 3 h / 85 °C / Inert atmosphere; Sealed tube 2: trifluoroacetic acid / dichloromethane / 2 h / 23 °C
  • 2
  • [ 1620828-90-1 ]
  • [ 211943-13-4 ]
  • [ 1620828-94-5 ]
YieldReaction ConditionsOperation in experiment
127 mg With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; caesium carbonate In tetrahydrofuran; water at 85℃; for 3h; Inert atmosphere; Sealed tube; 48.1 Example 48 (4S,6S)-4-(5-(5-(lH-tetrazol-5-yl)pyridin-3-yl)-2-fluorophenyl)-4-(fluoromethyl)-6- (trifluoromethyl)-5,6-dihydro-4H-l,3-oxazin-2-amine Step 1 : To a solution of (4S,6S)-N-(bis(4-methoxyphenyl)(phenyl)methyl)-4-(5-(5,5- dimethyl-l,3,2-dioxaborinan-2-yl)-2-fluorophenyl)-4-(fluoromethyl)-6-(trifluoromethyl)-5,6- dihydro-4H-l,3-oxazin-2-amine (Intermediate XXXIX-1, 223 mg) in THF (8.00 ml) and water (4.00 ml) was added at room temperature 3-bromo-5-(lH-tetrazol-5-yl)pyridine (CAS 211943- 13-4,107 mg) and cesium carbonate (410 mg). Under argon 1,1'- bis(diphenylphosphino)ferrocene-palladium(II)dichloride dichloromethane complex (25.7 mg) was added and the 2-phase-reaction mixture was stirred in a sealed tube at 85 °C for 3 hours. The aqueous layer was separated and extracted with ethyl acetate. The combined organic layers were dried over Na2S04, filtered and evaporated. The residue was chromatographed (Si02, 0-80% MeOH in dichloromethane) to give (4S,6S)-4-(5-(5-(lH-tetrazol-5-yl)pyridin-3-yl)-2- fluorophenyl)-N-(bis(4-methoxyphenyl)(phenyl)methyl)-4-(fluoromethyl)-6-(trifluoromethyl)- 5,6-dihydro-4H-l,3-oxazin-2-amine (127 mg) as brown oil.
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