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[ CAS No. 751-03-1 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 751-03-1
Chemical Structure| 751-03-1
Structure of 751-03-1 * Storage: {[proInfo.prStorage]}
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Quality Control of [ 751-03-1 ]

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Product Details of [ 751-03-1 ]

CAS No. :751-03-1 MDL No. :MFCD00075888
Formula : C26H30O7 Boiling Point : -
Linear Structure Formula :- InChI Key :MAYJEFRPIKEYBL-OASIGRBWSA-N
M.W : 454.51 Pubchem ID :119041
Synonyms :
AI3-37934;CCRIS 8657

Calculated chemistry of [ 751-03-1 ]

Physicochemical Properties

Num. heavy atoms : 33
Num. arom. heavy atoms : 5
Fraction Csp3 : 0.65
Num. rotatable bonds : 1
Num. H-bond acceptors : 7.0
Num. H-bond donors : 0.0
Molar Refractivity : 116.73
TPSA : 95.34 Ų

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : Yes
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.83 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.93
Log Po/w (XLOGP3) : 3.16
Log Po/w (WLOGP) : 3.6
Log Po/w (MLOGP) : 2.16
Log Po/w (SILICOS-IT) : 4.12
Consensus Log Po/w : 3.19

Druglikeness

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

Water Solubility

Log S (ESOL) : -4.69
Solubility : 0.00918 mg/ml ; 0.0000202 mol/l
Class : Moderately soluble
Log S (Ali) : -4.83
Solubility : 0.00668 mg/ml ; 0.0000147 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -5.57
Solubility : 0.00123 mg/ml ; 0.00000271 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 6.39

Safety of [ 751-03-1 ]

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 [ 751-03-1 ]

* 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.

  • Upstream synthesis route of [ 751-03-1 ]
  • Downstream synthetic route of [ 751-03-1 ]

[ 751-03-1 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 751-03-1 ]
  • [ 1180-71-8 ]
YieldReaction ConditionsOperation in experiment
76%
Stage #1: at 60℃; for 3 h;
Stage #2: With sodium tetrahydroborate In tetrahydrofuran; methanol at 0℃; for 1 h;
0 ° C to acetic anhydride (100 mL) Slowly adding chromium trioxide (11 g, 110 mmol), To be stirred until orange, The addition of the raw material Obacunone (45 g, 99.1 mmol) And the temperature was raised to 60 ° C. The reaction was continued for 3 hours. TLC (PE: EA = 2: 1) was used to monitor the reaction end. After completion of the reaction, the reaction solution was concentrated and the concentrate was separated by ethyl acetate (200 mL) and water (200 mL) The organic phase was dried over magnesium sulfate and concentrated. Intermediate 2 (46.0 g, 98.2 mmol) was dissolved in tetrahydrofuran (200 mL) and methanol (20 mL). Sodium borohydride (6.0 g, 150 mmol) was slowly added at 0 ° C, TLC (PE: EA = 1: 1) showed the end of the reaction, the reaction was concentrated and the concentrate was extracted with ethyl acetate (200 mL), and the reaction was concentrated at 0 ° C for 1 hour. ), Washed successively with saturated sodium bicarbonate (100 mL), water (100 mL), and saturated brine (100 mL). The organic phase was concentrated by drying over magnesium sulfate and the remaining crude product was purified by flash silica gel to give intermediate 3 (33.0 g, 70.2 mmol) was dissolved in tetrahydrofuran (100 mL), and the eluent was petroleum ether (PE): ethyl acetate (EA) = 1: 1; And methanol (100 mL) were added lithium hydroxide (2.4 g, 100 mmol). The reaction was stirred at room temperature for 3 hours. TLC (PE: EA = 1: 1) showed that the reaction material disappeared and the reaction product was adjusted to pH = 5 to 6, ethyl acetate (2 x 100 mL). The combined organic phases were dried over magnesium sulfate, filtered and concentrated to give crude intermediate 4 (24.0 g, 71percent yield). Intermediate 4 (24.0 g, 49.2 (DE) (10.5 g, 60.0 mmol) was added dropwise to a solution of anhydrous tetrahydrofuran (300 mL) under nitrogen,15.7 g, 60.0 mmol) was added and the reaction was stirred at room temperature under nitrogen for 16 hours. TLC (PE: EA = 1: 1) was monitored and the reaction was complete. After completion of the reaction, the mixture was washed with saturated brine (3 x 50 mL) The organic phase was concentrated by suction over magnesium sulfate and the resulting residue was purified by flash silica gel column to give intermediate 5 (18.0 g, yield 78percent). The eluent was petroleum ether (PE): ethyl acetate (EA) 2: 1; Intermediate 5 (18.0 g, 38.3 mmol) was dissolved in anhydrous tetrahydrofuran (200 mL) and a solution of borane tetrahydrofuran (50 mL, 1 M in THF, 50 mmol) was slowly added dropwise. After stirring for 16 hours, H2O2 (50 mL) and saturated sodium bicarbonate solution (50 mL) were added to the reaction solution. The reaction was continued at room temperature for 2 hours. The reaction solution was separated and the aqueous phase was passed through ethyl acetate (3 x 50 mL), the combined organic phases were dried over magnesium sulfate and concentrated by filtration. The resulting residue was purified by flash silica gel column to give product intermediate 6 (11.0 g, yield 58percent) eluting with petroleum ether (PE): ethyl acetate (EA) = 4: 1; (DE) (5.9 g, 33.8 mmol), triphenylphosphine (8.9 g, 33 mmol) were added in anhydrous tetrahydrofuran (300 mL) under nitrogen under reduced pressure (11.0 g, 22.5 mmol) 33.8 mmol). The reaction was stirred at room temperature under nitrogen for 16 hours. TLC (PE: EA = 1: 1) was monitored. The reaction was complete and washed with saturated brine (3 x 50 mL). The organic phase was dried over magnesium sulfate The resulting residue was recrystallized from ethanol to give the final product limonin (8.0 g, yield 76percent).
Reference: [1] Patent: CN107027748, 2017, A, . Location in patent: Paragraph 0028
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