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[ CAS No. 28797-48-0 ] {[proInfo.proName]}

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Chemical Structure| 28797-48-0
Chemical Structure| 28797-48-0
Structure of 28797-48-0 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 28797-48-0 ]

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Product Citations

Product Details of [ 28797-48-0 ]

CAS No. :28797-48-0 MDL No. :MFCD21648226
Formula : C14H10ClN3O2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :RMBZFWLMYVPNGI-UHFFFAOYSA-N
M.W : 287.70 Pubchem ID :120053
Synonyms :

Calculated chemistry of [ 28797-48-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 20
Num. arom. heavy atoms : 15
Fraction Csp3 : 0.07
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 77.96
TPSA : 67.75 ?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) : -7.46 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.8
Log Po/w (XLOGP3) : 0.84
Log Po/w (WLOGP) : 2.32
Log Po/w (MLOGP) : 2.48
Log Po/w (SILICOS-IT) : 2.7
Consensus Log Po/w : 2.03

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.58
Solubility : 0.764 mg/ml ; 0.00265 mol/l
Class : Soluble
Log S (Ali) : -1.85
Solubility : 4.11 mg/ml ; 0.0143 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -5.1
Solubility : 0.00228 mg/ml ; 0.00000793 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 2.24

Safety of [ 28797-48-0 ]

Signal Word:Warning Class:
Precautionary Statements:P280-P305+P351+P338-P310 UN#:
Hazard Statements:H302-H315-H319-H332-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 28797-48-0 ]

* 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 [ 28797-48-0 ]

[ 28797-48-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 6789-94-2 ]
  • [ 28797-48-0 ]
  • 11-[(1-Ethyl-3-piperidyl)aminoacetyl]-5,11-dihydro-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one [ No CAS ]
YieldReaction ConditionsOperation in experiment
58% With sodium carbonate; In ethanol; EXAMPLE 10 11-[(1-Ethyl-3-piperidyl)aminoacetyl]-5,11-dihydro-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one 7.2 gm of 11-chloroacetyl-5,11-dihydro-6H-pyrido [2,3-b][1,4]benzodiazepin-6-one, 2.8 gm of sodium carbonate and 3.8 gm of <strong>[6789-94-2]1-ethyl-3-amino-piperidine</strong> were refluxed in 100 ml of ethanol for 5 hours. Then the hot mixture was suction-filtered, the filtrate was evaporated in vacuo to dryness, and the residue was purified on a silica gel column. The evaporation residue of the elude was recrystallized from ethyl acetate. M.p.: 147-148 C. Yield: 58% of theory.
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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 ? 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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