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[ CAS No. 118811-07-7 ] {[proInfo.proName]}

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Chemical Structure| 118811-07-7
Chemical Structure| 118811-07-7
Structure of 118811-07-7 * Storage: {[proInfo.prStorage]}

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Product Details of [ 118811-07-7 ]

CAS No. :118811-07-7 MDL No. :MFCD06796535
Formula : C17H25NO5S Boiling Point : No data available
Linear Structure Formula :- InChI Key :IKOMRHLHPZAEMV-UHFFFAOYSA-N
M.W : 355.45 Pubchem ID :15734713
Synonyms :

Calculated chemistry of [ 118811-07-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 24
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.59
Num. rotatable bonds : 6
Num. H-bond acceptors : 5.0
Num. H-bond donors : 0.0
Molar Refractivity : 95.26
TPSA : 81.29 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : Yes
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.33 cm/s

Lipophilicity

Log Po/w (iLOGP) : 3.56
Log Po/w (XLOGP3) : 3.01
Log Po/w (WLOGP) : 3.8
Log Po/w (MLOGP) : 2.51
Log Po/w (SILICOS-IT) : 1.69
Consensus Log Po/w : 2.91

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.73
Solubility : 0.0663 mg/ml ; 0.000187 mol/l
Class : Soluble
Log S (Ali) : -4.38
Solubility : 0.0148 mg/ml ; 0.0000415 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -3.8
Solubility : 0.0563 mg/ml ; 0.000158 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 3.15

Safety of [ 118811-07-7 ]

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

Application In Synthesis of [ 118811-07-7 ]

* 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 [ 118811-07-7 ]

[ 118811-07-7 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 18362-30-6 ]
  • [ 118811-07-7 ]
  • [ 867216-37-3 ]
YieldReaction ConditionsOperation in experiment
With potassium carbonate; In DMF (N,N-dimethyl-formamide); at 60℃; tert-Butyl 4-(tosyloxy)piperidine-1-carboxylate (1.42 g, 4.0 mmol) and 2-chloro-6- hydroxybenzaldehyde (620 mg, 3.3 mmol) were dissolved in N,N-dimethylformamide (20 mL) and potassium carbonate (552 mg, 4.0 mmol ) was added. The reaction mixture was allowed to stir at 60 °C overnight. Ice was added and the mixture was acidified with 6N hydrochloric acid. The mixture was extracted with ethyl acetate and the organic layer was washed with brine. The organic solution was dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The resulting residue was purified by column chromatography, on silica gel, eluting with 2: 8 ethyl acetate: hexanes to give tert-butyl 4-(3-chloro-2-formylphenoxy)piperidine-1- carboxylate (430 mg) as a white solid. 1H NMR (CDCI3): 10.50 (s, 1H), 7.35 (t, 1H), 7.05 (d, 1H), 6.90 (d, 1H), 4.60 (m, 1H), 3.65 (m, 2H), 3.45 (m, 2H), 1.85 (m, 4H),1.40 ppm (s, 9H).
  • 2
  • [ 22717-55-1 ]
  • [ 118811-07-7 ]
  • tert-butyl 4-(5-chloro-2-(methoxycarbonyl)phenoxy)piperidine-1-carboxylate [ No CAS ]
YieldReaction ConditionsOperation in experiment
75.68% With tetrabutylammomium bromide; potassium carbonate; In acetone;Reflux; To a stirred solution of methyl4-chloro-2-hydroxybenzoate (1.0 g, 5.35 mmol, 1.0 eq)in acetone (10 mL) was added K2C03 (3.69 g, 26.75 mmol, 5.0 eq) followed by tert-butyl 4-(tosyloxy)piperidine-1-carboxylate (step 1, 2.85 g, 8.039 mmol, 1.5 eq) and tetra-nbutylammoniumbromide (0.344 g, 1.07 mmol, 0.2 eq). The reaction mixture was heated to25 reflux for overnight. After completion of the reaction (monitored by TLC), the reactionmixture was evaporated under reduced pressure, diluted with water (20 mL) and extractedwith DCM (3x30 mL). The organic layer was washed with brine solution (20 mL), dried oversodium sulfate, filtered and evaporated under reduced pressure. The residue was purified bysilica gel column chromatography by using 0-3% methanol in dichloromethane gradient. Thefractions containing the expected product were combined and concentrated under reduced5 pressure to obtain the title compound (1.5 g, yield: 75.68%) as a colourless liquid. 1H NMR(300 MHz, CDCb): 8 ppm 7.80 (d, J = 8.1 Hz, IH), 7.34 (d, J = 8.1 Hz, IH), 6.97 (d, J = 7.2Hz, IH), 4.73-4.56 (m, IH), 3.87 (s, 3H), 3.64-3.50 (m, 3H), 3.30-3.20 (m, IH), 1.90-1.60(m, 4H), 1.47 (s, 9H); LC-MS: m/z 370.10 (M+Ht.
  • 3
  • [ 22717-55-1 ]
  • [ 118811-07-7 ]
  • 2-((1-(tert-butoxycarbonyl)piperidin-4-yl)oxy)-4-chlorobenzoic acid [ No CAS ]
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