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[ CAS No. 52763-21-0 ] {[proInfo.proName]}

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Chemical Structure| 52763-21-0
Chemical Structure| 52763-21-0
Structure of 52763-21-0 * Storage: {[proInfo.prStorage]}

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Product Details of [ 52763-21-0 ]

CAS No. :52763-21-0 MDL No. :MFCD00012792
Formula : C15H20ClNO3 Boiling Point : No data available
Linear Structure Formula :- InChI Key :UQOMEAWPKSISII-UHFFFAOYSA-N
M.W : 297.78 Pubchem ID :2723880
Synonyms :
Chemical Name :Ethyl 1-benzyl-3-oxopiperidine-4-carboxylate hydrochloride

Calculated chemistry of [ 52763-21-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 20
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.47
Num. rotatable bonds : 5
Num. H-bond acceptors : 4.0
Num. H-bond donors : 0.0
Molar Refractivity : 81.9
TPSA : 46.61 ?2

Pharmacokinetics

GI absorption : Low
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) : -6.01 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 2.96
Log Po/w (WLOGP) : -1.78
Log Po/w (MLOGP) : 1.69
Log Po/w (SILICOS-IT) : 2.41
Consensus Log Po/w : 1.06

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.44
Solubility : 0.107 mg/ml ; 0.000361 mol/l
Class : Soluble
Log S (Ali) : -3.6
Solubility : 0.0745 mg/ml ; 0.00025 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.67
Solubility : 0.0638 mg/ml ; 0.000214 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 2.38

Safety of [ 52763-21-0 ]

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

Application In Synthesis of [ 52763-21-0 ]

* 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 [ 52763-21-0 ]

[ 52763-21-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 52763-21-0 ]
  • [ 57297-29-7 ]
  • 7-benzyl-2-cyclopropyl-5,6,7,8-tetrahydropyrido[3,4-d]pyrimidin-4(3H)-one [ No CAS ]
YieldReaction ConditionsOperation in experiment
99% With sodium methylate; In methanol; at 25℃; for 20h;Inert atmosphere; General procedure: To a solution of sodium methoxide (25 wt-percent in methanol) (67.6 mL, 296 mmol) and methanol (70 mL) at 25 °C was added formamidine acetate (11.00 g, 106 mmol) and then ethyl N-benzyl-3-oxo-4-piperidine carboxylate hydrochloride (25.16 g, 84 mmol). The resulting mixture was stirred at 25 °C for 20 h. The mixture was cooled to 0 °C. Water (90mL) was added, followed by the dropwise addition of acetic acid (6.05 mL, 106 mmol), and the reaction mixture was stirred at 25 °C for another 3 h. The mixture was reduced in volume under vacuum until most of the methanol had been removed. The suspension was filtered. The solids were washed with water and thendried under vacuum to afford 7-benzyl-5,6,7,8-tetrahydropyrido[3,4-d]pyrimidin-4(3H)-one (16.10 g, 79 percent) as an off-white solid; LC/MS:m/z 242.06 (M + H)+, 0.598 min (method 12). 1H-NMR (500 MHz, CDCl3) delta12.61 (br s, 1 H), 7.99 (s, 1 H), 7.38-7.26 (m, 5 H),3.73 (m, 2 H), 3.50 (m, 2 H), 2.74 (m, 2 H), 2.66 (m, 2 H).
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