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[ CAS No. 374930-88-8 ] {[proInfo.proName]}

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Chemical Structure| 374930-88-8
Chemical Structure| 374930-88-8
Structure of 374930-88-8 * Storage: {[proInfo.prStorage]}

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Product Details of [ 374930-88-8 ]

CAS No. :374930-88-8 MDL No. :MFCD07375175
Formula : C13H19BrN4O2 Boiling Point : -
Linear Structure Formula :- InChI Key :UKCBGXCNXOKVTF-UHFFFAOYSA-N
M.W : 343.22 Pubchem ID :21914476
Synonyms :

Calculated chemistry of [ 374930-88-8 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 20
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.62
Num. rotatable bonds : 4
Num. H-bond acceptors : 4.0
Num. H-bond donors : 0.0
Molar Refractivity : 86.93
TPSA : 58.56 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.97 cm/s

Lipophilicity

Log Po/w (iLOGP) : 3.2
Log Po/w (XLOGP3) : 2.01
Log Po/w (WLOGP) : 1.53
Log Po/w (MLOGP) : 1.51
Log Po/w (SILICOS-IT) : 1.26
Consensus Log Po/w : 1.9

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.19
Solubility : 0.22 mg/ml ; 0.000642 mol/l
Class : Soluble
Log S (Ali) : -2.87
Solubility : 0.466 mg/ml ; 0.00136 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.15
Solubility : 0.242 mg/ml ; 0.000706 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 2.68

Safety of [ 374930-88-8 ]

Signal Word:Warning Class:
Precautionary Statements:P280-P305+P351+P338 UN#:
Hazard Statements:H317-H319 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 374930-88-8 ]

* 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 [ 374930-88-8 ]

[ 374930-88-8 ] Synthesis Path-Downstream   1~2

  • 2
  • [ 374930-88-8 ]
  • [ 116332-54-8 ]
  • tert-butyl 4-(5-(4-fluorobenzoyl)pyrimidin-2-yl)piperazine-1-carboxylate [ No CAS ]
YieldReaction ConditionsOperation in experiment
To a solution of tert-butyl 4-(5-bromopyrimidin-2-yl)piperazine-1-carboxylate (50 g, 146.2 mmol) in anhydrous THF (700 mL) was dropwise added n-BuLi (2.5 M in hexane, 70 mL, 175 mmol) at -78 C. under nitrogen. The mixture was stirred at -78 C. for 1 h, followed by the addition of a solution of <strong>[116332-54-8]4-fluoro-N-methoxy-N-methylbenzamide</strong> (30 g, 163.9 mmol) in anhydrous THF (100 mL). After stirred at -78 C. for another 2 h, the reaction mixture was quenched with saturated aqueous NH4Cl (250 mL) and extracted with ethyl acetate (200 mL*3). The combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo. The residue was diluted with propan-2-ol (150 mL) and stirred at RT for 30 mins. The solid was collected via filtration, washed with propan-2-ol (100 mL) and petroleum ether (300 mL), and dried under vacuum to give the title compound (26 g, yield 46%) as a yellow solid. MS (ES+) C20H23FN4O3 requires: 386. found 331 [M-56+H]+; purity: 100% (UV214).
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