Home Cart 0 Sign in  

[ CAS No. 870281-82-6 ] {[proInfo.proName]}

,{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]}
Chemical Structure| 870281-82-6
Chemical Structure| 870281-82-6
Structure of 870281-82-6 * Storage: {[proInfo.prStorage]}
Cart0 Add to My Favorites Add to My Favorites Bulk Inquiry Inquiry Add To Cart

Quality Control of [ 870281-82-6 ]

Related Doc. of [ 870281-82-6 ]

Alternatived Products of [ 870281-82-6 ]

Product Details of [ 870281-82-6 ]

CAS No. :870281-82-6 MDL No. :MFCD19443647
Formula : C22H18FN7O Boiling Point : -
Linear Structure Formula :- InChI Key :IFSDAJWBUCMOAH-HNNXBMFYSA-N
M.W : 415.42 Pubchem ID :11625818
Synonyms :
CAL-101;GS-1101;GS-1101, Idelalisib.

Calculated chemistry of [ 870281-82-6 ]

Physicochemical Properties

Num. heavy atoms : 31
Num. arom. heavy atoms : 25
Fraction Csp3 : 0.14
Num. rotatable bonds : 5
Num. H-bond acceptors : 6.0
Num. H-bond donors : 2.0
Molar Refractivity : 115.95
TPSA : 101.38 Ų

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : Yes
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : Yes
CYP2D6 inhibitor : Yes
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.21 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.7
Log Po/w (XLOGP3) : 3.69
Log Po/w (WLOGP) : 3.66
Log Po/w (MLOGP) : 2.88
Log Po/w (SILICOS-IT) : 3.48
Consensus Log Po/w : 3.28

Druglikeness

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

Water Solubility

Log S (ESOL) : -5.01
Solubility : 0.00409 mg/ml ; 0.00000984 mol/l
Class : Moderately soluble
Log S (Ali) : -5.51
Solubility : 0.00129 mg/ml ; 0.0000031 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -8.29
Solubility : 0.00000212 mg/ml ; 0.0000000051 mol/l
Class : Poorly soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 2.0
Synthetic accessibility : 3.86

Safety of [ 870281-82-6 ]

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 [ 870281-82-6 ]

* 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 [ 870281-82-6 ]
  • Downstream synthetic route of [ 870281-82-6 ]

[ 870281-82-6 ] Synthesis Path-Upstream   1~18

  • 1
  • [ 870281-86-0 ]
  • [ 87-42-3 ]
  • [ 870281-82-6 ]
YieldReaction ConditionsOperation in experiment
3.1 g With triethylamine In <i>tert</i>-butyl alcohol at 30 - 85℃; for 24 h; (S)-2-(1 -aminopropyl)-5-fluoro-3-phenylquinazolin-4(3H)-one prepared in example 26 (4.2 g) and t-Butanol (21 mL) were charged into a 100 mL round bottom flask. Triethylamine (3.91 mL) and 6-Chloropurine (2.5 g) were added at 30 00. The resultant reaction mixture was heated to85°C and stirred for 24 hours. The reaction mixture was evaporated completely under reduced pressure at 40°C. The resultant residue was diluted with water (100 mL) and stirred for 30 minutes. The precipitate was filtered and the solid was washed with water (30 mL) and n-Hexane (50 mL) and dried for 1 hour under vacuum. The crude was purified by chromatographyusing Si02 (1 00:200) (solvent MeOH: DCM: TEA:: 5: 94: 1). The eluted fractions were evaporated completely under vacuum. The isolated product was diluted in dichloromethane (100 mL) and the organic layer was washed with brine solution (2x25 mL). The organic layer dried over sodium sulphate (10 g) and evaporated under reduced pressure to yield 3.1 g of Idelalisib as pale yellow solid.Purity: 97.87percent by HPLC; chiral purity: 98.77percent by H PLC
Reference: [1] Patent: WO2016/108206, 2016, A2, . Location in patent: Page/Page column 49; 50
  • 2
  • [ 870281-86-0 ]
  • [ 767-69-1 ]
  • [ 870281-82-6 ]
YieldReaction ConditionsOperation in experiment
62.5 g With N-ethyl-N,N-diisopropylamine In <i>tert</i>-butyl alcohol at 85 - 90℃; Example 6:Preparation of 5-fluoro-3-phenyl-2-[(15)-l-(7H-purin-6-ylamino)propyl]- 4(3H)-quinazolinone [idelalisib] A mixture of 2-(l-aminopropyl)-5-fluoro-3-phenyl-3H-quinazolin-4-one (50 g, 0.17 mole) and 6-bromopurine (37.5 g, 0.18 mole) was taken in tert-butanol (500 mL). To this solution, 43.4 g DIPEA [Ν,Ν,-diisopropylethylamine] was added and the reaction mixture was stirred at 85 °C- 90 °C for 20 to 25 hours. After completion of the reaction, the reaction mixture was concentrated by distillation under vacuum and the residue was dissolved in methanol (500 mL). This solution was slowly added to water (5000 mL) and stirred for next 40 to 60 minutes. The solid was filtered then sucked dried. Finally, the solid was dried at 50 °C- 55 °C under vacuum for 4 to 5 hours to get 5-fluoro-3-phenyl-2-[(15)-l-(7H-purin-6-ylamino)propyl]-4(3H)- quinazolinone (idelalisib) (62.5 g, 89percent molar).
Reference: [1] Patent: WO2016/147206, 2016, A1, . Location in patent: Page/Page column 16
  • 3
  • [ 62-53-3 ]
  • [ 870281-82-6 ]
Reference: [1] RSC Advances, 2018, vol. 8, # 28, p. 15863 - 15869
  • 4
  • [ 62-53-3 ]
  • [ 870281-82-6 ]
Reference: [1] Patent: WO2016/108206, 2016, A2,
[2] Patent: WO2016/108206, 2016, A2,
[3] RSC Advances, 2018, vol. 8, # 28, p. 15863 - 15869
  • 5
  • [ 870281-83-7 ]
  • [ 870281-82-6 ]
Reference: [1] Patent: WO2016/108206, 2016, A2,
[2] Patent: WO2016/108206, 2016, A2,
[3] RSC Advances, 2018, vol. 8, # 28, p. 15863 - 15869
  • 6
  • [ 7304-32-7 ]
  • [ 870281-82-6 ]
Reference: [1] RSC Advances, 2018, vol. 8, # 28, p. 15863 - 15869
  • 7
  • [ 385-02-4 ]
  • [ 870281-82-6 ]
Reference: [1] Patent: WO2016/108206, 2016, A2,
[2] Patent: WO2016/108206, 2016, A2,
  • 8
  • [ 870281-84-8 ]
  • [ 870281-82-6 ]
Reference: [1] Patent: WO2016/108206, 2016, A2,
[2] Patent: WO2016/108206, 2016, A2,
  • 9
  • [ 870281-85-9 ]
  • [ 870281-82-6 ]
Reference: [1] Patent: WO2016/108206, 2016, A2,
[2] Patent: WO2016/108206, 2016, A2,
  • 10
  • [ 21802-46-0 ]
  • [ 870281-82-6 ]
Reference: [1] Patent: WO2016/108206, 2016, A2,
  • 11
  • [ 66224-66-6 ]
  • [ 870281-82-6 ]
Reference: [1] Patent: WO2016/108206, 2016, A2,
  • 12
  • [ 1229622-81-4 ]
  • [ 870281-82-6 ]
Reference: [1] Patent: WO2016/108206, 2016, A2,
  • 13
  • [ 78755-94-9 ]
  • [ 870281-82-6 ]
Reference: [1] Patent: WO2016/147206, 2016, A1,
  • 14
  • [ 434-76-4 ]
  • [ 870281-82-6 ]
Reference: [1] Patent: WO2016/147206, 2016, A1,
  • 15
  • [ 87-42-3 ]
  • [ 870281-82-6 ]
Reference: [1] Patent: CN106279171, 2017, A,
  • 16
  • [ 851165-38-3 ]
  • [ 870281-82-6 ]
Reference: [1] Patent: CN108409740, 2018, A,
  • 17
  • [ 1229622-72-3 ]
  • [ 870281-82-6 ]
Reference: [1] Patent: WO2016/108206, 2016, A2,
  • 18
  • [ 870281-86-0 ]
  • [ 5451-40-1 ]
  • [ 870281-82-6 ]
Reference: [1] Patent: WO2016/108206, 2016, A2,
Same Skeleton Products
Historical Records

Similar Product of
[ 870281-82-6 ]

Chemical Structure| 1453810-72-4

A632590[ 1453810-72-4 ]

(S)-2-(1-((9H-Purin-6-yl)amino)propyl)-5-fluoro-3-phenylquinazolin-4(3H)-one xhydrochloride

Reason: Free-salt