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[ CAS No. 135065-69-9 ] {[proInfo.proName]}

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Chemical Structure| 135065-69-9
Chemical Structure| 135065-69-9
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Product Details of [ 135065-69-9 ]

CAS No. :135065-69-9 MDL No. :MFCD03426270
Formula : C10H19NO4 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 217.26 Pubchem ID :-
Synonyms :

Calculated chemistry of [ 135065-69-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 15
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.9
Num. rotatable bonds : 4
Num. H-bond acceptors : 4.0
Num. H-bond donors : 1.0
Molar Refractivity : 58.84
TPSA : 59.0 ?2

Pharmacokinetics

GI absorption : High
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) : -7.54 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.59
Log Po/w (XLOGP3) : 0.12
Log Po/w (WLOGP) : 0.23
Log Po/w (MLOGP) : 0.03
Log Po/w (SILICOS-IT) : 0.33
Consensus Log Po/w : 0.66

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.0
Solubility : 21.8 mg/ml ; 0.1 mol/l
Class : Very soluble
Log S (Ali) : -0.91
Solubility : 26.4 mg/ml ; 0.122 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -0.57
Solubility : 58.2 mg/ml ; 0.268 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 3.14

Safety of [ 135065-69-9 ]

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

Application In Synthesis of [ 135065-69-9 ]

* 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 [ 135065-69-9 ]

[ 135065-69-9 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 24424-99-5 ]
  • [ 40987-24-4 ]
  • [ 135065-69-9 ]
YieldReaction ConditionsOperation in experiment
99% palladium-carbon; In methanol; Step A: 2-Hydroxymethylmorpholine-4-carboxylic acid tert-butyl ester To a solution of (4-benzylmorpholin-2-yl)-methanol (0.66 g, 3.18 mmol, Synth. Comm. 1980, 10, 59-73) in MeOH (20 mL) was added Boc anhydride (0.83 g, 3.82 mmol) followed by Pd/C (0.66 g, 6.20 mmol). The mixture was stirred under hydrogen atmosphere for 60 hours. The catalyst was removed by filtration and the filtrate was concentrated under reduced pressure to afford the product as colorless oil (0.69 g, 99% yield).
87% Ammonium formate (3.04 g, 48.2 mmol) and 10% palladium on activated carbon (500 mg) were added to (4-benzylmorpholin-2-yl)methanol (1.00 g, 4.82 mmol) in methanol (50 mL). The mixture was stirred at room temperature for 4 hours. Subsequently, the reaction mixture was filtered through Celite and the solvent was evaporated. The resulting residue was dissolved in acetonitrile (20 mL). While this solution was chilled in an ice bath, ditert-butyl dicarbonate (1.58 g, 7.23 mmol) and triethylamine (1.35 mL, 9.64 mmol) were added and the mixture was stirred at room temperature for 3 hours. The solvent was evaporated and water was added to the residue. The mixture was then extracted with ethyl acetate and the extract was washed with brine, followed by drying over magnesium sulfate and evaporation of the solvent. Purification of the residue by silica gel column chromatography (hexane: ethyl acetate = 5:1 -> 1:1) gave 907 mg (87%) of the desired compound as a colorless oil. 1H NMR (400MHz, DMSO-d6) delta 1.40 (9H, s), 2.47-2.66 (1H, m), 2.73-2.92 (1H, m),3.25-3.45 (4H, m), 3.70 (1H, d, J = 13.4 Hz), 3.79 (1H, dd, J = 11.6, 2.4 Hz), 3.85 (1H, d, J = 12.8 Hz), 4.77 (1H, t, J = 5.5 Hz).
  • 2
  • [ 40987-24-4 ]
  • [ 135065-69-9 ]
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