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[ CAS No. 1350643-72-9 ] {[proInfo.proName]}

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Chemical Structure| 1350643-72-9
Chemical Structure| 1350643-72-9
Structure of 1350643-72-9 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 1350643-72-9 ]

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Product Details of [ 1350643-72-9 ]

CAS No. :1350643-72-9 MDL No. :MFCD23166427
Formula : C17H15ClN2O Boiling Point : -
Linear Structure Formula :- InChI Key :MZINZXIFJMLTOK-NSHDSACASA-N
M.W : 298.77 Pubchem ID :66607319
Synonyms :

Calculated chemistry of [ 1350643-72-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 21
Num. arom. heavy atoms : 16
Fraction Csp3 : 0.12
Num. rotatable bonds : 2
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 87.04
TPSA : 48.02 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : Yes
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.01 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.61
Log Po/w (XLOGP3) : 2.97
Log Po/w (WLOGP) : 3.34
Log Po/w (MLOGP) : 3.47
Log Po/w (SILICOS-IT) : 3.54
Consensus Log Po/w : 3.19

Druglikeness

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

Water Solubility

Log S (ESOL) : -4.0
Solubility : 0.0302 mg/ml ; 0.000101 mol/l
Class : Soluble
Log S (Ali) : -3.64
Solubility : 0.0682 mg/ml ; 0.000228 mol/l
Class : Soluble
Log S (SILICOS-IT) : -5.98
Solubility : 0.000311 mg/ml ; 0.00000104 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 2.93

Safety of [ 1350643-72-9 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 1350643-72-9 ]

* 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 [ 1350643-72-9 ]

[ 1350643-72-9 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 1350643-72-9 ]
  • [ 1201438-56-3 ]
  • 2
  • [ 1350643-72-9 ]
  • [ 7306-68-5 ]
  • [ 1201438-56-3 ]
  • 3
  • [ 1350643-72-9 ]
  • [ 628692-15-9 ]
  • [ 1420627-92-4 ]
YieldReaction ConditionsOperation in experiment
With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; sodium carbonate; In N,N-dimethyl acetamide; water; at 120℃; for 16h;Sealed tube; 0740] To a mixture of ? (S)-3-(1-aminoethyl)-8-chloro-2-phenylisoquinolin-1(2H)-one 1 (1.41 g, 4.72 mmol) and ? <strong>[628692-15-9](2-methoxypyrimidin-5-yl)boronic acid</strong> (1.09 g, 7.08 mmol) in anhydrous ? DMA (20 mL) in a sealed tube, ? PdCl2(dppf) (309 mg, 0.38 mmol) and ? aqueous Na2CO3 solution (1 M, 14.2 mL, 14.2 mmol) were added and the resulting mixture was stirred at 120° C. for 16 h. The reaction mixture was allowed to cool to RT, quenched with water, and then extracted with ethyl acetate. The combined organic layers were washed with brine, dried over Na2SO4 and filtered. The filtrate was concentrated in vacuo and the residue was slurried in ether for 10 min. The solid was collected by filtration, rinsed with ether and dried in vacuo to afford a first amount of product 2. The filtrate was concentrated in vacuo and the residue was further purified by ISCO column chromatography using a silica gel cartridge and eluting with 0-8percent MeOH-DCM to afford a second amount of product 2.
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Technical Information

? Acyl Group Substitution ? Alkyl Halide Occurrence ? Baeyer-Villiger Oxidation ? Barbier Coupling Reaction ? Baylis-Hillman Reaction ? Bucherer-Bergs Reaction ? Buchwald-Hartwig C-N Bond and C-O Bond Formation Reactions ? Chan-Lam Coupling Reaction ? Clemmensen Reduction ? Complex Metal Hydride Reductions ? Corey-Bakshi-Shibata (CBS) Reduction ? Corey-Chaykovsky Reaction ? Fischer Indole Synthesis ? General Reactivity ? Grignard Reaction ? Henry Nitroaldol Reaction ? Hiyama Cross-Coupling Reaction ? Horner-Wadsworth-Emmons Reaction ? Hydride Reductions ? Kinetics of Alkyl Halides ? Kumada Cross-Coupling Reaction ? Lawesson's Reagent ? Leuckart-Wallach Reaction ? Mannich Reaction ? McMurry Coupling ? Meerwein-Ponndorf-Verley Reduction ? Passerini Reaction ? Paternò-Büchi Reaction ? Petasis Reaction ? Peterson Olefination ? Pictet-Spengler Tetrahydroisoquinoline Synthesis ? Preparation of Aldehydes and Ketones ? Preparation of Amines ? Prins Reaction ? Reactions of Aldehydes and Ketones ? Reactions of Alkyl Halides with Reducing Metals ? Reactions of Amines ? Reactions of Benzene and Substituted Benzenes ? Reformatsky Reaction ? Robinson Annulation ? Schlosser Modification of the Wittig Reaction ? Schmidt Reaction ? Specialized Acylation Reagents-Carbodiimides and Related Reagents ? Specialized Acylation Reagents-Ketenes ? Specialized Acylation Reagents-Vilsmeier Reagent ? Stille Coupling ? Stobbe Condensation ? Substitution and Elimination Reactions of Alkyl Halides ? Suzuki Coupling ? Tebbe Olefination ? Ugi Reaction ? Wittig Reaction ? Wolff-Kishner Reduction
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