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[ CAS No. 571189-16-7 ] {[proInfo.proName]}

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Chemical Structure| 571189-16-7
Chemical Structure| 571189-16-7
Structure of 571189-16-7 * Storage: {[proInfo.prStorage]}

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Product Details of [ 571189-16-7 ]

CAS No. :571189-16-7 MDL No. :MFCD11849291
Formula : C14H20N4O4 Boiling Point : -
Linear Structure Formula :- InChI Key :SUWKOEMQNOBJEQ-UHFFFAOYSA-N
M.W : 308.33 Pubchem ID :11243758
Synonyms :

Calculated chemistry of [ 571189-16-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 22
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.57
Num. rotatable bonds : 5
Num. H-bond acceptors : 5.0
Num. H-bond donors : 0.0
Molar Refractivity : 90.26
TPSA : 91.49 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.9 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.62
Log Po/w (XLOGP3) : 1.8
Log Po/w (WLOGP) : 1.29
Log Po/w (MLOGP) : 0.99
Log Po/w (SILICOS-IT) : -1.02
Consensus Log Po/w : 1.14

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.76
Solubility : 0.539 mg/ml ; 0.00175 mol/l
Class : Soluble
Log S (Ali) : -3.34
Solubility : 0.141 mg/ml ; 0.000457 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.07
Solubility : 2.61 mg/ml ; 0.00847 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 2.94

Safety of [ 571189-16-7 ]

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 [ 571189-16-7 ]

* 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 [ 571189-16-7 ]

[ 571189-16-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 52092-47-4 ]
  • [ 57260-71-6 ]
  • [ 571189-16-7 ]
YieldReaction ConditionsOperation in experiment
63.81% With potassium carbonate; In dimethyl sulfoxide; at 100 - 110℃;Microwave irradiation; A microwave vial was charged with <strong>[52092-47-4]5-chloro-2-nitropyridine</strong> (1 g, 6.31 mmol), 1 -boc-piperazine (1 .29g, 6.94mmol) and potassium carbonate (3.3ml_, 18.92mmol), which was suspended in DMSO (15ml_). The resulting mixture was irradiated for 1 hour at 100°C. After this time, the mixture had solidified. LC-MS showed the reaction had not gone to completion. The solid mixture was then transferred to a flask along with DMSO (5ml_) and heated to 1 10°C, at which point the solid mixture had melted. This was left heating overnight, after which LC-MS showed product formation and no starting material. Reaction was allowed to cool. The reaction mixture was then added to water and extracted with EtOAc (x3). The organics were then combined, washed with brine, dried over sodium sulfate, filtered and concentrated to dryness, affording an orange solid. Purification by flash column chromatography was then performed, (40g S1O2, eluting with 0-50percent EtOAc in heptane). The fractions containing product were combined and concentrated to dryness, affording tert-butyl 4-(6- nitro-3-pyridyl)piperazine-1 -carboxylate (1 .24g, 4.02mmol, 63.81 percent yield) as a bright orange/yellow solid. MS Method 2: RT: 1 .61 min, ES+ m/z 309.1 [M+H]+ H NMR (400MHz, CDC ) delta/ppm: 8.10-8.13 (d, J=9.1 Hz, 1 H), 8.06-8.07 (d, J=3.0Hz, 1 H), 7.12-7.16 (dd, J=9.2, 3.0Hz, 1 H), 3.55-3.59 (m, 4H), 3.36-3.41 (m, 4H), 1 .42 (s, 9H).
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