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[ CAS No. 1235451-62-3 ] {[proInfo.proName]}

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Chemical Structure| 1235451-62-3
Chemical Structure| 1235451-62-3
Structure of 1235451-62-3 * Storage: {[proInfo.prStorage]}
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Product Details of [ 1235451-62-3 ]

CAS No. :1235451-62-3 MDL No. :MFCD18383572
Formula : C19H28BNO4 Boiling Point : -
Linear Structure Formula :- InChI Key :JNLQPCDEHQJZLY-UHFFFAOYSA-N
M.W : 345.24 Pubchem ID :66977628
Synonyms :

Calculated chemistry of [ 1235451-62-3 ]

Physicochemical Properties

Num. heavy atoms : 25
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.63
Num. rotatable bonds : 4
Num. H-bond acceptors : 4.0
Num. H-bond donors : 0.0
Molar Refractivity : 103.85
TPSA : 48.0 Ų

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : Yes
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : Yes
CYP3A4 inhibitor : Yes
Log Kp (skin permeation) : -5.79 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 3.69
Log Po/w (WLOGP) : 2.9
Log Po/w (MLOGP) : 2.33
Log Po/w (SILICOS-IT) : 2.27
Consensus Log Po/w : 2.24

Druglikeness

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

Water Solubility

Log S (ESOL) : -4.22
Solubility : 0.0209 mg/ml ; 0.0000604 mol/l
Class : Moderately soluble
Log S (Ali) : -4.39
Solubility : 0.0141 mg/ml ; 0.0000409 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -4.75
Solubility : 0.00618 mg/ml ; 0.0000179 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 3.62

Safety of [ 1235451-62-3 ]

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 [ 1235451-62-3 ]

* 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 [ 1235451-62-3 ]

[ 1235451-62-3 ] Synthesis Path-Downstream   1~3

YieldReaction ConditionsOperation in experiment
84% With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium acetate; In 1,4-dioxane; at 85.0℃;Inert atmosphere; General procedure: Step 34b: N-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetamide (Compound 0602-107)[0334]To a solution of compound 0601-107 (2.5 g, 11.6 mmol) and bis(pinacolato)diboron (4.4 g, 17.5 mmol) in dioxane (100 mL) was added potassium acetate (3.4 g, 35 mmol) and PdCl2(dppf)2 (0.95 g, 1.1 mmol). The mixture was degassed with nitrogen and heated at 85 C. for overnight. The reaction mixture was concentrated under reduced pressure to afford the crude product, which purified by column chromatography (ethyl acetate in petroleum ether, 15% v/v) to give the compound 0602-107 (1.55 g, 51%) as a pink solid. LCMS: 262 [M+1]+. 1H NMR (400 MHz, DMSO-d6) delta 1.29 (s, 12H), 2.03 (s, 3H), 7.30 (s, 1H), 7.31 (d, J=2.0 Hz 1H), 7.73 (d, J=2.0 Hz, 1H), 7.89 (d, J=1.6 Hz, 1H), 9.93 (s, 1H).
84% With palladium bis[bis(diphenylphosphino)ferrocene] dichloride; potassium acetate; In 1,4-dioxane; at 85.0℃;Inert atmosphere; General procedure: Compound in dioxane (100mL) 0601-107 (2.5g, 11.6mmol) and a solution of bis (pinacolato) diboron (4.4 g, 17.5 mmol), potassium acetate (3.4 g, 35 mmol) and and PdCl2 (dppf) 2 ( 0.95g, 1.1mmol) was added. The mixture was degassed with nitrogen and heated overnight at 85 C.. The reaction mixture was concentrated under reduced pressure to give the crude product, which was purified by column chromatography (petroleum ether in ethyl acetate, 15% v / v) to give the compound 0602-107 as a pink solid obtained (1.55 g, 51%).
With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium acetate; In 1,4-dioxane; at 100.0℃; for 5.0h;Inert atmosphere; General procedure: A solution of 1 .6 (600 mg, 1 .8 mmol), KOAc (265 mg, 2.7 mmol), Pin2B2 (503 mg, 1 .98 mmol) and PdCI2(dppf) (132 mg, 0.18 mmol) in dioxane (20 mL) was stirred at 100 C for 5 hr under nitrogen protection. The mixture was concentrated in vacuum to afford black syrup, it was used for the next directl . LC-MS: [M+H]+ = 381 .0.
  • 2
  • tert-butyl 4-((diethoxyphosphoryl)oxy)indoline-1-carboxylate [ No CAS ]
  • [ 73183-34-3 ]
  • [ 1235451-62-3 ]
  • 3
  • tert-butyl 4-hydroxyindoline-1-carboxylate [ No CAS ]
  • [ 1235451-62-3 ]
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