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[ CAS No. 1014645-87-4 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 1014645-87-4
Chemical Structure| 1014645-87-4
Structure of 1014645-87-4 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 1014645-87-4 ]

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Product Citations

Product Details of [ 1014645-87-4 ]

CAS No. :1014645-87-4 MDL No. :MFCD11616336
Formula : C11H14ClNO2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :SZUAJCIGBDCCPA-UHFFFAOYSA-N
M.W : 227.69 Pubchem ID :66824369
Synonyms :

Calculated chemistry of [ 1014645-87-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 15
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.36
Num. rotatable bonds : 3
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 59.74
TPSA : 52.32 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : Yes
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.03 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 2.34
Log Po/w (WLOGP) : 2.05
Log Po/w (MLOGP) : 1.85
Log Po/w (SILICOS-IT) : 2.0
Consensus Log Po/w : 1.65

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.82
Solubility : 0.342 mg/ml ; 0.0015 mol/l
Class : Soluble
Log S (Ali) : -3.08
Solubility : 0.19 mg/ml ; 0.000835 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.94
Solubility : 0.264 mg/ml ; 0.00116 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.38

Safety of [ 1014645-87-4 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 1014645-87-4 ]

* 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 [ 1014645-87-4 ]

[ 1014645-87-4 ] Synthesis Path-Upstream   1~8

  • 1
  • [ 1006037-03-1 ]
  • [ 1014645-87-4 ]
YieldReaction ConditionsOperation in experiment
100% With hydrogenchloride In diethyl ether; ethyl acetate Step 2:To a solution of ER-886774-00 (1.63 g, 0.0085 mol) in ethyl acetate (10 mL) was added 2.0 M of hydrogen chloride in Ether (6.0 mL, 0.012 mol). After stirring for several minutes, the reaction mixture was concentrated to give the title compound (quantitative yield) as pale brown solid.
68.7 g With hydrogenchloride In ethyl acetate at 20℃; for 2 h; To a cooled solution of methyl 4-(1-aminocyclopropyl)benzoate (D6) (100 g, 524 mmol) in ethyl acetate (500 ml) 4N HCl (g)/ethyl acetate solution (300 ml) was added and the resulting mixture was stirred at room temperature for 2 hours. Evaporated the solvent, the residue was recrystallized with petroleum ether/EtOAc to afford the title compound (D7) (68.7 g) as a white solid.
Reference: [1] Patent: WO2012/39972, 2012, A1, . Location in patent: Page/Page column 39
[2] Journal of Organic Chemistry, 2010, vol. 75, # 12, p. 4078 - 4085
[3] Patent: WO2012/76063, 2012, A1, . Location in patent: Page/Page column 39
[4] Patent: US2013/261100, 2013, A1, . Location in patent: Paragraph 0273-0274; 02796
  • 2
  • [ 1338243-88-1 ]
  • [ 1014645-87-4 ]
YieldReaction ConditionsOperation in experiment
5.3 g With hydrogenchloride In ethyl acetate at 20℃; To a cooled solution of methyl 4-(1-((tert-butoxycarbonyl)amino)cyclopropyl)benzoate (D5) (7.4 g, 25.4 mmol) in ethyl acetate (10 ml) HCl (g)/ethyl acetate (4N, 50 ml) was added the mixture was stirred at room temperature overnight. Evaporated the solvent, the residue was washed with petroleum ether to afford the title compound (D7) (5.3 g) as a white solid.
Reference: [1] Patent: WO2012/76063, 2012, A1, . Location in patent: Page/Page column 38-39
[2] Patent: US2013/261100, 2013, A1, . Location in patent: Paragraph 0273-0275
  • 3
  • [ 67-56-1 ]
  • [ 1014645-83-0 ]
  • [ 1014645-87-4 ]
Reference: [1] Patent: WO2008/17164, 2008, A1, . Location in patent: Page/Page column 59
  • 4
  • [ 345965-52-8 ]
  • [ 1014645-87-4 ]
Reference: [1] Patent: WO2012/76063, 2012, A1,
  • 5
  • [ 360773-84-8 ]
  • [ 1014645-87-4 ]
Reference: [1] Patent: WO2012/76063, 2012, A1,
  • 6
  • [ 67-56-1 ]
  • [ 1014645-75-0 ]
  • [ 1014645-87-4 ]
Reference: [1] Bioorganic and Medicinal Chemistry Letters, 2010, vol. 20, # 12, p. 3760 - 3763
  • 7
  • [ 1014743-82-8 ]
  • [ 1014645-87-4 ]
Reference: [1] Patent: WO2012/39972, 2012, A1,
  • 8
  • [ 1129-35-7 ]
  • [ 1014645-87-4 ]
Reference: [1] Patent: WO2012/76063, 2012, A1,
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