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[ CAS No. 628692-15-9 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 628692-15-9
Chemical Structure| 628692-15-9
Structure of 628692-15-9 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 628692-15-9 ]

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Product Details of [ 628692-15-9 ]

CAS No. :628692-15-9 MDL No. :MFCD03094664
Formula : C5H7BN2O3 Boiling Point : No data available
Linear Structure Formula :- InChI Key :YPWAJLGHACDYQS-UHFFFAOYSA-N
M.W : 153.93 Pubchem ID :2736778
Synonyms :

Calculated chemistry of [ 628692-15-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.2
Num. rotatable bonds : 2
Num. H-bond acceptors : 5.0
Num. H-bond donors : 2.0
Molar Refractivity : 38.35
TPSA : 75.47 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -7.66 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : -0.59
Log Po/w (WLOGP) : -1.84
Log Po/w (MLOGP) : -1.99
Log Po/w (SILICOS-IT) : -1.62
Consensus Log Po/w : -1.21

Druglikeness

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

Water Solubility

Log S (ESOL) : -0.69
Solubility : 31.1 mg/ml ; 0.202 mol/l
Class : Very soluble
Log S (Ali) : -0.52
Solubility : 46.1 mg/ml ; 0.299 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -0.66
Solubility : 34.1 mg/ml ; 0.221 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.13

Safety of [ 628692-15-9 ]

Signal Word:Warning Class:
Precautionary Statements:P264-P270-P280-P301+P312+P330-P305+P351+P338-P337+P313-P501 UN#:
Hazard Statements:H302-H319 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 628692-15-9 ]

* 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 [ 628692-15-9 ]

[ 628692-15-9 ] Synthesis Path-Downstream   1~11

  • 1
  • [ 1722-12-9 ]
  • [ 628692-15-9 ]
  • 2-methoxy-5-(2-pyrimidyl)pyrimidine [ No CAS ]
  • 2
  • [ 5332-24-1 ]
  • [ 628692-15-9 ]
  • 3-(2-methoxypyrimidin-5-yl)quinoline [ No CAS ]
  • 3
  • [ 13195-50-1 ]
  • [ 628692-15-9 ]
  • 2-methoxy-5-(5-nitrothien-2-yl)pyrimidine [ No CAS ]
  • 4
  • [ 4595-60-2 ]
  • [ 628692-15-9 ]
  • 2-methoxy-5-(2-pyrimidyl)pyrimidine [ No CAS ]
  • 6
  • [ 628692-15-9 ]
  • 2-[2-(3-iodo-phenyl)-2<i>H</i>-tetrazol-5-yl]-pyridine [ No CAS ]
  • 2-methoxy-5-[3-(5-pyridin-2-yl-tetrazol-2-yl)-phenyl]-pyrimidine [ No CAS ]
  • 7
  • [ 628692-15-9 ]
  • 2-[2-(3-fluoro-5-iodo-phenyl)-2<i>H</i>-tetrazol-5-yl]-pyridine [ No CAS ]
  • 5-[3-fluoro-5-(5-pyridin-2-yl-tetrazol-2-yl)-phenyl]-2-methoxy-pyrimidine [ No CAS ]
  • 8
  • [ 954123-48-9 ]
  • [ 628692-15-9 ]
  • 2-methoxy-5-(3-(((4-phenylpiperidin-4-yl)methoxy)methyl)-5-(trifluoromethyl)phenyl)pyrimidine [ No CAS ]
YieldReaction ConditionsOperation in experiment
EXAMPLE 1 2-Methoxy-5-(3-(((4-phenylpiperidin-4-yl)methoxy)methyl)-5-(trifluoromethyl)phenyl)pyrimidine. tert-Butyl 4-((3-bromo-5-(trifluoromethyl)benzyloxy)methyl)-4-phenylpiperidine-1-carboxylate (60. 0 mg, 0.11 mmol), 2-methoxy-5-pyridine boronic acid (72.0 mg, 0.47 mmol), and tetrakis(triphenylphosphine) palladium(0) (17.1 mg, 0.011 mmol) were combined in dry tetrahydrofuran (2 mL) in a microwave tube and sealed. The mixture was flushed with nitrogen then 0.35 mL of a 1 N potassium hydroxide aqueous solution was introduced. The mixture was heated at 120° C. for 1 h via microwave. After cooling to room temperature, the reaction mixture was concentrated and treated with a trifluoroacetic acid/methylene chloride mixture (1:1, 2 mL) for 1 h. The solvent was removed in vacuo and the resulting crude mixture passed through a strong cation exchange column. After washing the column with several volumes of methanol, the product was eluted by washing the column with 2 M ammonia in methanol. Concentration and preparative HPLC afforded 21.0 mg (42percent) of the desired compound as its TFA salt. 1H-NMR (CDCl3, 500 MHz) delta 8.57 (s, 2H), 7.54 (s, 1H), 7.25-7.31 (m, 8H), 4.40 (s, 2H), 4.03 (s, 3H), 3.40 (s, 2H), 2.83-2.88 (m, 2H), 2.64-2.69 (m, 2H), 2.10-2.18 (m, 2H), 1.77-1.86 (m, 2H). Mass spec.: 458.18 (MH)+.
  • 9
  • [ 958852-14-7 ]
  • [ 628692-15-9 ]
  • [ 958852-15-8 ]
YieldReaction ConditionsOperation in experiment
95% With potassium carbonate;tetrakis(triphenylphosphine) palladium(0); In 1,4-dioxane; water; at 100℃; for 8h; A mixture of 6-(methyloxy)-3-pyridinyl]boronic acid (225 mg, 1.5 mmol), 4- iodo-6-quinolinecarbaldehyde (283 mg, 1 mmol), tetrakistriphenylphosphine palladium (0) (57 mg, 0.05 mmol), 2 M aqueous K2CO3 (2.5 ml. of a 2 M solution), and dioxane (5 ml.) ) was heated at 100 0C for 8 h and cooled to room temperature. The dioxane was removed under reduced pressure and the residue dissolved in 2:1 mixture of methylene chloride/water and the solution filtered. The organic layer was separated and dried with sodium sulfate and the crude product obtained by decanting the solution and evaporation of the methylene chloride. The crude product was purified by silica gel chromatography eluting with methylene chloride/methanol (0-1percent methanol gradient) to give the title compound (250 mg, 95 percent). MS(ES)+ m/e 265 [M+H]+.
  • 10
  • [ 628692-15-9 ]
  • 3-(4-aminophenyl)-7-(2-methoxy-5-pyrimidinyl)thieno[3,2-c]pyridin-4-amine [ No CAS ]
YieldReaction ConditionsOperation in experiment
EXAMPLE 133A 3-(4-aminophenyl)-7-(2-methoxy-5-pyrimidinyl)thieno[3,2-c]pyridin-4-amine The desired product was prepared by substituting 2-methoxy-5-pyrimidinylboronic acid for 4-pyridylboronic acid in Examples 121A-B. MS (ESI(+)) m/e 350 (M+H)+.
  • 11
  • [ 84249-14-9 ]
  • [ 628692-15-9 ]
  • C10H10N4O [ No CAS ]
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