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[ CAS No. 886779-69-7 ] {[proInfo.proName]}

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Chemical Structure| 886779-69-7
Chemical Structure| 886779-69-7
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Product Details of [ 886779-69-7 ]

CAS No. :886779-69-7 MDL No. :MFCD08686626
Formula : C10H17F3N2O2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :WCGKHZHOGLVVPU-UHFFFAOYSA-N
M.W : 254.25 Pubchem ID :66599850
Synonyms :

Calculated chemistry of [ 886779-69-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 17
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.9
Num. rotatable bonds : 4
Num. H-bond acceptors : 6.0
Num. H-bond donors : 1.0
Molar Refractivity : 63.5
TPSA : 41.57 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.69 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.56
Log Po/w (XLOGP3) : 1.64
Log Po/w (WLOGP) : 2.26
Log Po/w (MLOGP) : 1.3
Log Po/w (SILICOS-IT) : 1.23
Consensus Log Po/w : 1.8

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.19
Solubility : 1.66 mg/ml ; 0.00652 mol/l
Class : Soluble
Log S (Ali) : -2.13
Solubility : 1.9 mg/ml ; 0.00748 mol/l
Class : Soluble
Log S (SILICOS-IT) : -1.94
Solubility : 2.94 mg/ml ; 0.0116 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 2.97

Safety of [ 886779-69-7 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 886779-69-7 ]

* 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 [ 886779-69-7 ]

[ 886779-69-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 24424-99-5 ]
  • [ 131922-05-9 ]
  • [ 886779-69-7 ]
YieldReaction ConditionsOperation in experiment
90% In dichloromethane; at 20℃; for 3h; To a solution of <strong>[131922-05-9]2-(trifluoromethyl)piperazine</strong> (135 mg, 0.876 mmol) in DCM (6 ml) were added di-tert-butyl dicarbonate (0.224 ml, 0.963 mmol) and the resulting mixture was stirred at RT for 3 h, then concentrated and the residue was purified via silica gel chromatography (0 - 100 % EtOAc in hexanes) to give tert-butyl 3 -(trifluoromethyl)piperazine-l -carboxylate (200 mg, 0.787 mmol, 90 % yield) as a pale yellow solid. MS (ES+) C10H17F3N2O2 requires: 254, found: 155 [M+H]+- Boc group.
3.2 g In tetrahydrofuran; at 20℃; for 14h; Into a 250-mL round-bottom flask, was placed <strong>[131922-05-9]2-(trifluoromethyl)piperazine</strong> (4.00 g, crude), THF (100.00 mL), Boc2O (8.50 g, 38.947 mmol, 1.50 equiv). The resulting solution was stirred for 14 hr at room temperature. The resulting mixture was concentrated. The residue was applied onto a silica gel column and purified with ethyl acetate/petroleum ether (1:1). This resulted in 3.2 g (48.50%) of tert-butyl 3-(trifluoromethyl)piperazine-1-carboxylate as a white solid. H-NMR: (300 MHz, Chloroform-d) δ 4.13 (d, J = 16.2 Hz, 1H), 3.94 - 3.74 (m, 1H), 3.24 (dtd, J = 10.2, 6.6, 3.0 Hz, 1H), 3.16 - 2.87 (m, 3H), 2.78 (td, J = 12.7, 11.7, 4.8 Hz, 1H), 2.07 (s, 1H), 1.49 (s, 9H).
3.2 g In tetrahydrofuran; at 20℃; for 14h; Into a 250-mL round-bottom flask, was placed <strong>[131922-05-9]2-(trifluoromethyl)piperazine</strong> (4.00 g, crude), THF (100.00 mL), Boc2O (8.50 g, 38.947 mmol, 1.50 equiv). The resulting solution was stirred for 14 hr at room temperature. The resulting mixture was concentrated. The residue was applied onto a silica gel column and purified with ethyl acetate/petroleum ether (1:1). This resulted in 3.2 g (48.50%) of tert-butyl 3-(trifluoromethyl)piperazine-1-carboxylate as a white solid. H-NMR: (300 MHz, Chloroform-d) δ 4.13 (d, J = 16.2 Hz, 1H), 3.94 - 3.74 (m, 1H), 3.24 (dtd, J = 10.2, 6.6, 3.0 Hz, 1H), 3.16 - 2.87 (m, 3H), 2.78 (td, J = 12.7, 11.7, 4.8 Hz, 1H), 2.07 (s, 1H), 1.49 (s, 9H).
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