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[ CAS No. 87611-00-5 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 87611-00-5
Chemical Structure| 87611-00-5
Structure of 87611-00-5 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 87611-00-5 ]

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Product Details of [ 87611-00-5 ]

CAS No. :87611-00-5 MDL No. :MFCD09954883
Formula : C8H3Cl2FN2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :AXMYGHKVWFFYCR-UHFFFAOYSA-N
M.W : 217.03 Pubchem ID :34176231
Synonyms :

Calculated chemistry of [ 87611-00-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 10
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 49.52
TPSA : 25.78 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.1 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.26
Log Po/w (XLOGP3) : 3.56
Log Po/w (WLOGP) : 3.5
Log Po/w (MLOGP) : 2.85
Log Po/w (SILICOS-IT) : 3.61
Consensus Log Po/w : 3.15

Druglikeness

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

Water Solubility

Log S (ESOL) : -4.0
Solubility : 0.0218 mg/ml ; 0.000101 mol/l
Class : Soluble
Log S (Ali) : -3.79
Solubility : 0.0355 mg/ml ; 0.000163 mol/l
Class : Soluble
Log S (SILICOS-IT) : -4.85
Solubility : 0.00309 mg/ml ; 0.0000142 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 2.0
Synthetic accessibility : 1.84

Safety of [ 87611-00-5 ]

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

Application In Synthesis of [ 87611-00-5 ]

* 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 [ 87611-00-5 ]

[ 87611-00-5 ] Synthesis Path-Downstream   1~16

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YieldReaction ConditionsOperation in experiment
80.8% With 1,8-diazabicyclo[5.4.0]undec-7-ene; trichlorophosphate; In toluene; at 50 - 120℃; B-1 (2.6 g, 14.43 mmol) was suspended in 29 mL of toluene and heated to 50 C. Phosphoryl chloride (9.88 mL, 108.25 mmol) was added dropwise, and then DBU (4.31 mL, 28.87 mmol) was added dropwise. The mixture was stirred vigorously at 120 C for overnight. After the reaction mixture was cooled at room temperature, it was added dropwise to ice-water. The aqueous layer was extracted with ethyl acetate. After it was washed with brine and dried with Na2S04, it was concentrated to give a solid. The crude product was purified by column chromatography on silica gel eluting with toluene to yield 3.41 g (80.8%) of B-2 as a white powder. It was used for next reaction without purification.
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  • [ 769158-33-0 ]
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  • C21H20FN5O [ No CAS ]
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  • [ 1312784-33-0 ]
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  • [ 1312784-40-9 ]
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  • [ 321745-86-2 ]
  • [ 1312784-45-4 ]
YieldReaction ConditionsOperation in experiment
45% With dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane;palladium diacetate; In tetrahydrofuran; diethyl ether; at 45 - 48℃; for 40.0h;Inert atmosphere; Preparation of tert-butyl 2-(2-chloro-5-fluoroquinazolin-4-yl)acetate To a solution of <strong>[87611-00-5]2,4-dichloro-5-fluoroquinazoline</strong> (1.88 g, 8.64 mmol, Accela ChemBio) in THF (21.6 mL) under a nitrogen atmosphere was added (2-tert-butoxy-2-oxoethyl)zinc(II) chloride (0.5 M solution in Et2O, 51.8 mL, 25.9 mmol, Rieke Metals). Nitrogen was bubbled through the solution for about 20 min. Palladium(II) acetate (0.097 g, 0.432 mmol) and 2-dicyclohexylphosphino-2',6'-dimethoxybiphenyl (0.355 g, 0.864 mmol) were added to the reaction, each in one portion, and nitrogen was bubbled through the solution for about 5 min. The reaction solution was warmed to about 45 C. for about 24 h. After allowing to cool to ambient temperature, (2-tert-butoxy-2-oxoethyl)zinc(II) chloride (0.5 M solution in Et2O, 20.0 mL, 10.0 mmol, Rieke Metals), Pd(OAc)2 (0.097 g, 0.432 mmol), and 2-dicyclohexylphosphino-2',6'-dimethoxybiphenyl (0.355 g, 0.864 mmol) were added respectively. Nitrogen was bubbled through the solution for about 20 min and the reaction was warmed to about 48 C. for about 16 h. After cooling to ambient temperature, saturated aqueous NaHCO3 (90 mL) and EtOAc (100 mL) were added. The solid was removed by filtration. The layers were separated and the aqueous phase was extracted with EtOAc (100 mL). The combined organics were dried over MgSO4, filtered, and concentrated under reduced pressure. The residue was purified by flash column chromatography on silica gel eluting with a gradient of 0-30% EtOAc in heptane. The product containing fractions were concentrated under reduced pressure and the residue was triturated with EtOAc. The solid was removed by filtration and the organics were concentrated under reduced pressure to afford tert-butyl 2-(2-chloro-5-fluoroquinazolin-4-yl)acetate (1.14 g, 45% yield): LC/MS (Table 1, method c) Rt=2.64 min; MS m/z: 297 (M+H)+.
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  • [ 1312783-59-7 ]
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  • [ 434-76-4 ]
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