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[ CAS No. 364794-80-9 ] {[proInfo.proName]}

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Chemical Structure| 364794-80-9
Chemical Structure| 364794-80-9
Structure of 364794-80-9 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 364794-80-9 ]

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Product Details of [ 364794-80-9 ]

CAS No. :364794-80-9 MDL No. :MFCD06797489
Formula : C17H26BNO3 Boiling Point : No data available
Linear Structure Formula :- InChI Key :RCGRLLZELIIKDH-UHFFFAOYSA-N
M.W : 303.20 Pubchem ID :2795578
Synonyms :

Calculated chemistry of [ 364794-80-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 22
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.65
Num. rotatable bonds : 3
Num. H-bond acceptors : 4.0
Num. H-bond donors : 0.0
Molar Refractivity : 92.89
TPSA : 30.93 ?2

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) : -6.47 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 2.37
Log Po/w (WLOGP) : 1.29
Log Po/w (MLOGP) : 1.3
Log Po/w (SILICOS-IT) : 2.19
Consensus Log Po/w : 1.43

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.22
Solubility : 0.184 mg/ml ; 0.000607 mol/l
Class : Soluble
Log S (Ali) : -2.66
Solubility : 0.663 mg/ml ; 0.00219 mol/l
Class : Soluble
Log S (SILICOS-IT) : -4.58
Solubility : 0.00807 mg/ml ; 0.0000266 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 3.17

Safety of [ 364794-80-9 ]

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

Application In Synthesis of [ 364794-80-9 ]

* 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 [ 364794-80-9 ]

[ 364794-80-9 ] Synthesis Path-Downstream   1~4

  • 2
  • [ 364794-80-9 ]
  • [ 364793-60-2 ]
  • 4-(2,4-Dichloro-5-methoxyanilino)-7-[3-(4-morpholinylmethyl)-phenyl]-3-quinolinecarbonitrile [ No CAS ]
  • 3
  • [ 364794-80-9 ]
  • [ 364793-73-7 ]
  • 4-(2,4-Dichloro-5-methoxyanilino)-6-methoxy-7-[3-(4-morpholinylmethyl]phenyl }-3-quinolinecarbonitrile [ No CAS ]
  • 4
  • [ 956034-15-4 ]
  • [ 364794-80-9 ]
  • C21H23ClN4O2S [ No CAS ]
YieldReaction ConditionsOperation in experiment
With sodium carbonate;bis-triphenylphosphine-palladium(II) chloride; In water; acetonitrile; at 100℃; for 0.166667 - 0.666667h;Microwave irradiation; Example 223 2-(lH-indazol-4-yl)-4-morpholino-6-(3-(morpholinomethyl)phenyl)thieno[3,2-d]pyrimidine 299[00823] 2-Chloro-6-iodo-4-morpholinothieno[3,2-£/lpyrimidine 19 (50 mg) was <n="215"/>coupled to 4-[3-(4,4,5,5-tetramethyl-l,332-dioxaborolan-2-yl)]benzylmorpholine, and then reacted with 4-(4,4,5,5-tetramemyl-l,3,2-dioxaborolan-2-yl)-17Wndazole 7 via GeneralProcedure F. The product was purified by reverse phase HPLC to yield 2.6 mg of 299. MS.(Ql) 513.2 (M)+; General Procedure F Suzuki coupling reactions in one pot[00245] 2-CMoro-64odo-4rmorpholmothieno[3,2-£?]pyrimidine 19 (leq), phenylboronic acid or heterocycleboronic acid (R1 -B(OH)2, 1.1 eq) and bis(triphenylphosphine)palladium(II) dichloride (O.leq) in lMNa2CC>3 aqueous solution (3 eq) and acetonitrile (3eq) was heated to 100 0C in a sealed microwave reactor for 10 to 40 min to give 20. Upon completion, 4-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)-lH- indazole 7 (1.3 eq) and bis(triphenylphosphine)palladium(II) dichloride (O.leq) were added in the same pot. The reaction mixture was heated to 150 0C in a sealed microwave reactor for 10 to 15min. The mixture was extracted with ethyl acetate (3 x 5 mL). The combined organic layers were concentrated to yield crude 21.
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