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[ CAS No. 144072-30-0 ] {[proInfo.proName]}

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Chemical Structure| 144072-30-0
Chemical Structure| 144072-30-0
Structure of 144072-30-0 * Storage: {[proInfo.prStorage]}

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Product Citations

Product Details of [ 144072-30-0 ]

CAS No. :144072-30-0 MDL No. :MFCD06245541
Formula : C12H15NO3 Boiling Point : No data available
Linear Structure Formula :- InChI Key :SVQVBAUJEKSBEC-UHFFFAOYSA-N
M.W : 221.25 Pubchem ID :2771821
Synonyms :

Calculated chemistry of [ 144072-30-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 16
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.33
Num. rotatable bonds : 5
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 62.08
TPSA : 55.4 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.78 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.27
Log Po/w (XLOGP3) : 2.64
Log Po/w (WLOGP) : 2.66
Log Po/w (MLOGP) : 1.72
Log Po/w (SILICOS-IT) : 1.88
Consensus Log Po/w : 2.23

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.82
Solubility : 0.333 mg/ml ; 0.0015 mol/l
Class : Soluble
Log S (Ali) : -3.45
Solubility : 0.0778 mg/ml ; 0.000351 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.31
Solubility : 0.11 mg/ml ; 0.000495 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.84

Safety of [ 144072-30-0 ]

Signal Word:Warning Class:
Precautionary Statements:P261 UN#:
Hazard Statements:H302-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 144072-30-0 ]

* 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 [ 144072-30-0 ]

[ 144072-30-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 144072-30-0 ]
  • [ 6882-68-4 ]
  • tert-butyl (4-((E)-((41S,7aR,13aR,13bR)-10-oxydehydro-1H,5H,8H-dipyridine[2,1-f:3',2',1'-ij][1,6]naphthyridine-11(10H)-ylidene)methyl)phenyl)carbamate [ No CAS ]
YieldReaction ConditionsOperation in experiment
73% With sodium hydride; In N,N-dimethyl-formamide; at 0℃; for 2h; Add 5mL of dry DMF and 28.8mg (1.20mmol) of sodium hydride into a 25mL round bottom flask, stir well, add 248.36mg (1.00mmol) of <strong>[6882-68-4]sophoridine</strong>, keep at 0C and then add 4-(Boc-amino) Benzaldehyde 265.50 mg (1.20 mmol), stirred and reacted for 2 hours. After the reaction is complete, add 40 mL of water,It was extracted three times with 50 mL of dichloromethane, the organic phases were combined, washed with saturated brine, and an appropriate amount of anhydrous sodium sulfate was added for sufficient drying. The crude product was obtained after evaporation under reduced pressure, which was purified by silica gel column chromatography. The eluent was dichloro Methane: methanol (20:1), 329.67 mg of yellow oil was obtained, and the yield was 73%.
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Technical Information

? Acyl Group Substitution ? Barbier Coupling Reaction ? Baylis-Hillman Reaction ? Benzylic Oxidation ? Birch Reduction ? Blanc Chloromethylation ? 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-Chaykovsky Reaction ? Corey-Fuchs Reaction ? Fischer Indole Synthesis ? Friedel-Crafts Reaction ? Grignard Reaction ? Hantzsch Dihydropyridine Synthesis ? Henry Nitroaldol Reaction ? Horner-Wadsworth-Emmons Reaction ? Hydride Reductions ? Hydrogenolysis of Benzyl Ether ? Julia-Kocienski Olefination ? Knoevenagel Condensation ? Lawesson's Reagent ? Leuckart-Wallach Reaction ? Mannich Reaction ? McMurry Coupling ? Meerwein-Ponndorf-Verley Reduction ? Mukaiyama Aldol Reaction ? Nozaki-Hiyama-Kishi Reaction ? Passerini Reaction ? Paternò-Büchi Reaction ? Petasis Reaction ? Pictet-Spengler Tetrahydroisoquinoline Synthesis ? Preparation of Aldehydes and Ketones ? Preparation of Alkylbenzene ? Preparation of Amines ? Prins Reaction ? Reactions of Aldehydes and Ketones ? Reactions of Amines ? Reactions of Benzene and Substituted Benzenes ? Reformatsky Reaction ? Schlosser Modification of the Wittig Reaction ? Schmidt Reaction ? Specialized Acylation Reagents-Carbodiimides and Related Reagents ? Specialized Acylation Reagents-Ketenes ? Specialized Acylation Reagents-Vilsmeier Reagent ? Stetter Reaction ? Stobbe Condensation ? Tebbe Olefination ? Ugi Reaction ? Vilsmeier-Haack Reaction ? Wittig Reaction ? Wolff-Kishner Reduction
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