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[ CAS No. 933757-00-7 ]

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3d Animation Molecule Structure of 933757-00-7
Chemical Structure| 933757-00-7
Chemical Structure| 933757-00-7
Structure of 933757-00-7 * Storage: {[proInfo.prStorage]}
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Product Details of [ 933757-00-7 ]

CAS No. :933757-00-7 MDL No. :MFCD26696351
Formula : C13H14N2O Boiling Point : -
Linear Structure Formula :- InChI Key :MXZLCDOTWPBHCM-UHFFFAOYSA-N
M.W :214.26 Pubchem ID :83489475
Synonyms :

Calculated chemistry of [ 933757-00-7 ]

Physicochemical Properties

Num. heavy atoms : 16
Num. arom. heavy atoms : 12
Fraction Csp3 : 0.15
Num. rotatable bonds : 3
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 64.12
TPSA : 48.02 Ų

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) : -6.68 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.23
Log Po/w (XLOGP3) : 1.3
Log Po/w (WLOGP) : 1.2
Log Po/w (MLOGP) : 1.61
Log Po/w (SILICOS-IT) : 2.04
Consensus Log Po/w : 1.68

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.34
Solubility : 0.969 mg/ml ; 0.00452 mol/l
Class : Soluble
Log S (Ali) : -1.91
Solubility : 2.64 mg/ml ; 0.0123 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -4.08
Solubility : 0.0178 mg/ml ; 0.000083 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.96

Safety of [ 933757-00-7 ]

Signal Word:Warning Class:
Precautionary Statements:P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313 UN#:
Hazard Statements:H315-H319 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 933757-00-7 ]

* 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.

  • Downstream synthetic route of [ 933757-00-7 ]

[ 933757-00-7 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 20577-27-9 ]
  • [ 933757-00-7 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1: nickel(II) chloride hexahydrate; sodium tetrahydroborate / methanol / 4 h / 0 - 20 °C 2: potassium carbonate / N,N-dimethyl-formamide / 12 h / 0 - 20 °C 3: hydrogenchloride / 1,4-dioxane / 12 h / 20 °C
  • 2
  • [ 1614218-02-8 ]
  • [ 933757-00-7 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: potassium carbonate / N,N-dimethyl-formamide / 12 h / 0 - 20 °C 2: hydrogenchloride / 1,4-dioxane / 12 h / 20 °C
  • 3
  • [ 1614218-03-9 ]
  • [ 933757-00-7 ]
YieldReaction ConditionsOperation in experiment
90% With hydrogenchloride In 1,4-dioxane at 20℃; for 12h; 1.3 Step 3 : 3-(aminomethyl)-1-benzylpyridin-2( 111)-one Step 3 : 3-(aminomethyl)-1-benzylpyridin-2( 111)-one Tert-butyl ((1 -benzyl-2-oxo- 1 ,2-dihydropyridin-3-yl)methyl)carhamate (2.6 g. 0.00828 mol,Preparation 1,step-2) was dissolved in 4N 1,4-dioxane/HC1 (20 mL) and stirred at RT for about12 h. Excess solvent was removed in vaccuo and the crude material was triturated with ether (2 x100 inL) to afford 3-(aminornethyl)-1-benzylpyridiri-2(1H)-one 2.0 g (90 %) as off white solid.‘H NMR (400 MHz, DMSO-d6) : 8.187 (hs,IH), 7.937-7.915 (dd, J=21-{z,1H), 7.648-7.628 (dd, J=2Hz,1H), 7.350-7.289 (m,5H), 6.382-6.348 (t, J6.8Hz, IH), 5.171 (s,21-1). 3.858-3.8 15 (m2H), MS m/z : 428.3(M+F1)4,
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