Home Cart 0 Sign in  

[ CAS No. 1513879-19-0 ] {[proInfo.proName]}

,{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]}
Chemical Structure| 1513879-19-0
Chemical Structure| 1513879-19-0
Structure of 1513879-19-0 * Storage: {[proInfo.prStorage]}
Cart0 Add to My Favorites Add to My Favorites Bulk Inquiry Inquiry Add To Cart

Quality Control of [ 1513879-19-0 ]

Related Doc. of [ 1513879-19-0 ]

Alternatived Products of [ 1513879-19-0 ]

Product Details of [ 1513879-19-0 ]

CAS No. :1513879-19-0 MDL No. :MFCD28963927
Formula : C22H18ClN5O2 Boiling Point : -
Linear Structure Formula :- InChI Key :TYMFFISSODJRDV-UHFFFAOYSA-N
M.W : 419.86 Pubchem ID :90157166
Synonyms :

Calculated chemistry of [ 1513879-19-0 ]

Physicochemical Properties

Num. heavy atoms : 30
Num. arom. heavy atoms : 21
Fraction Csp3 : 0.09
Num. rotatable bonds : 6
Num. H-bond acceptors : 4.0
Num. H-bond donors : 1.0
Molar Refractivity : 115.54
TPSA : 79.6 Ų

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : Yes
CYP2D6 inhibitor : Yes
CYP3A4 inhibitor : Yes
Log Kp (skin permeation) : -6.3 cm/s

Lipophilicity

Log Po/w (iLOGP) : 3.04
Log Po/w (XLOGP3) : 3.61
Log Po/w (WLOGP) : 3.69
Log Po/w (MLOGP) : 1.99
Log Po/w (SILICOS-IT) : 2.75
Consensus Log Po/w : 3.01

Druglikeness

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

Water Solubility

Log S (ESOL) : -4.84
Solubility : 0.00608 mg/ml ; 0.0000145 mol/l
Class : Moderately soluble
Log S (Ali) : -4.97
Solubility : 0.00451 mg/ml ; 0.0000107 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -7.33
Solubility : 0.0000197 mg/ml ; 0.000000047 mol/l
Class : Poorly soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 2.0
Synthetic accessibility : 2.95

Safety of [ 1513879-19-0 ]

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

Application In Synthesis of [ 1513879-19-0 ]

* 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 [ 1513879-19-0 ]

[ 1513879-19-0 ] Synthesis Path-Downstream   1~6

  • 2
  • [4-(methylcarbamoyl)phenyl]boronic acid [ No CAS ]
  • [ 1607830-47-6 ]
  • [ 1513879-19-0 ]
YieldReaction ConditionsOperation in experiment
80.2% With potassium fluoride; tetrakis(triphenylphosphine) palladium(0) In 1,4-dioxane; 1,2-dimethoxyethane; water at 110℃; for 0.5h; Microwave irradiation;
With dipotassium hydrogenphosphate In tetrahydrofuran; water at 150℃; for 0.75h; Microwave irradiation; 228 N-(4-chlorophenyl)-N-methyl-3-[4-(methylcarbamoyl)phenyl]imidazo[1,2-a]pyrazine-6-carboxamide Pd-DPP (palladium diphenylphosphine supported on silica, Silicycle) (25 mg) was added to a solution of 3-bromo-N-(4-chlorophenyl)-N-methylimidazo[1 ,2-a]pyrazine-6-carboxamide (40 mg, 0.1 1 mmol), (4-(methylcarbamoyl)phenyl)boronic acid (50 mg, 0.28 mmol), K2HP04 (50 mg, 0.36 mmol), THF (2.0 mL) and water (1.0 mL). The reaction was heated in a microwave reactor at 150 °C for 45 minutes. After cooling to room temperature, the reaction was concentrated in vacuo. The crude material was purified by flash chromatography (silica, 0-15% methanol/chloroform). 1 H NMR (400 MHz, DMSO) δ 8.86 (s, 1 H), 8.81 (d, J = 1 .3, 1 H), 8.62 (d, J - 4.6, 1 H), 8.19 (s, 1 H), 8.05 (d, J = 8.4, 2H), 7.79 (d, J= 8.4, 2H), 7.35 (d, J= 8.8, 2H), 7.30 (d, J= 8.8, 2H), 3.42 (s, 3H), 2.84 (d, J= 4.5, 3H). 1 H NMR (400 MHz, DMSO) δ 8.86 (s, 1 H), 8.81 (d, J = 1 .3, 1 H), 8.62 (d, J = 4.6, 1 H), 8.19 (s, 1 H), 8.05 (d, J = 8.4, 2H), 7.79 (d, J = 8.4, 2H), 7.35 (d, J = 8.8, 2H), 7.30 (d, J = 8.8, 2H), 3.42 (s, 3H), 2.84 (d, J = 4.5, 3H);; MS m/z 420.2 (M+H)+; r.t. = 0.98.
  • 3
  • [ 588720-67-6 ]
  • [ 1513879-19-0 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 4 steps 1.1: N-Bromosuccinimide / dichloromethane / 3 h / 20 °C 2.1: sodium hydroxide / tetrahydrofuran; water / 1.5 h / 60 °C 3.1: oxalyl dichloride; N,N-dimethyl-formamide / dichloromethane / 0.5 h / 20 °C 3.2: 3 h / 20 °C 4.1: dipotassium hydrogenphosphate / tetrahydrofuran; water / 0.75 h / 150 °C / Microwave irradiation
Multi-step reaction with 5 steps 1: N-Bromosuccinimide / dichloromethane / 3 h / 20 °C 2: sodium hydroxide / tetrahydrofuran; water / 1.5 h / 60 °C 3: oxalyl dichloride; N,N-dimethyl-formamide / dichloromethane / 0.5 h / 20 °C 4: triethylamine / dichloromethane / 3 h / 20 °C 5: tetrakis(triphenylphosphine) palladium(0); potassium fluoride / 1,4-dioxane; water; 1,2-dimethoxyethane / 0.5 h / 110 °C / Microwave irradiation
  • 4
  • [ 1607829-61-7 ]
  • [ 1513879-19-0 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1.1: sodium hydroxide / tetrahydrofuran; water / 1.5 h / 60 °C 2.1: oxalyl dichloride; N,N-dimethyl-formamide / dichloromethane / 0.5 h / 20 °C 2.2: 3 h / 20 °C 3.1: dipotassium hydrogenphosphate / tetrahydrofuran; water / 0.75 h / 150 °C / Microwave irradiation
Multi-step reaction with 4 steps 1: sodium hydroxide / tetrahydrofuran; water / 1.5 h / 60 °C 2: oxalyl dichloride; N,N-dimethyl-formamide / dichloromethane / 0.5 h / 20 °C 3: triethylamine / dichloromethane / 3 h / 20 °C 4: tetrakis(triphenylphosphine) palladium(0); potassium fluoride / 1,4-dioxane; water; 1,2-dimethoxyethane / 0.5 h / 110 °C / Microwave irradiation
  • 5
  • [ 1234015-04-3 ]
  • [ 1513879-19-0 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1.1: oxalyl dichloride; N,N-dimethyl-formamide / dichloromethane / 0.5 h / 20 °C 1.2: 3 h / 20 °C 2.1: dipotassium hydrogenphosphate / tetrahydrofuran; water / 0.75 h / 150 °C / Microwave irradiation
Multi-step reaction with 3 steps 1: oxalyl dichloride; N,N-dimethyl-formamide / dichloromethane / 0.5 h / 20 °C 2: triethylamine / dichloromethane / 3 h / 20 °C 3: tetrakis(triphenylphosphine) palladium(0); potassium fluoride / 1,4-dioxane; water; 1,2-dimethoxyethane / 0.5 h / 110 °C / Microwave irradiation
Same Skeleton Products
Historical Records