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[ CAS No. 111196-81-7 ] {[proInfo.proName]}

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Chemical Structure| 111196-81-7
Chemical Structure| 111196-81-7
Structure of 111196-81-7 * Storage: {[proInfo.prStorage]}

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Product Details of [ 111196-81-7 ]

CAS No. :111196-81-7 MDL No. :MFCD00799503
Formula : C6H7ClN2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :BGLLZQRUXJGTAD-UHFFFAOYSA-N
M.W : 142.59 Pubchem ID :3572763
Synonyms :

Calculated chemistry of [ 111196-81-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.33
Num. rotatable bonds : 1
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 36.81
TPSA : 25.78 ?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) : -5.78 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.95
Log Po/w (XLOGP3) : 1.96
Log Po/w (WLOGP) : 1.69
Log Po/w (MLOGP) : 0.89
Log Po/w (SILICOS-IT) : 2.29
Consensus Log Po/w : 1.76

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -2.39
Solubility : 0.586 mg/ml ; 0.00411 mol/l
Class : Soluble
Log S (Ali) : -2.13
Solubility : 1.07 mg/ml ; 0.00747 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.04
Solubility : 0.132 mg/ml ; 0.000923 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.62

Safety of [ 111196-81-7 ]

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

Application In Synthesis of [ 111196-81-7 ]

* 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 [ 111196-81-7 ]

[ 111196-81-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 7037-49-2 ]
  • [ 111196-81-7 ]
  • [ 1046815-82-0 ]
YieldReaction ConditionsOperation in experiment
75% With potassium carbonate; In N,N-dimethyl-formamide; at 65℃; for 12h; (Step 6-3) Preparation of 3-(l -(5-ethylpyrimidin-2-yl)piperidin-4-yl)propan-l-ol 2-chloro-5-ethyl pyrimidine (1.0 g, 7.0 mmol) was dissolved in N,N-dimethyl formamide (DMF, 15 ml), and then 3-(piperidin-4-yl)propan-l -ol (1.1 g, 7.7 mmol) and potassium carbonate (K2C03, 2.9 g, 21.0 mmol) were added to the reaction solution. The reaction solution was stirred at 65 °C for 12 hours, and then diluted with water, and extracted with EA. Moisture was removed from an organic layer with MgSC^, the organic layer was filtered and concentrated under reduced pressure, and the residue was purified with silica gel column chromatography to obtain the desired form of the compound, 3-(l-(5-ethylpyrimidin-2-yl)piperidin-4-yl)propan-l -ol in a yield of 75percent. H MR(400MHz, CDC13) delta 8.15 (; s, 2H), 4.67 (d, 2H, J=13.6Hz), 2.87 (m, 2H), 2.83 (t, 2H, J=12.6 Hz), 2.44 (q, 2H, J=7.6Hz), 1.46-1.38 (m, 9H), 1.21 (t, 3H, J=7.6Hz)
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