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[ CAS No. 146844-02-2 ] {[proInfo.proName]}

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Chemical Structure| 146844-02-2
Chemical Structure| 146844-02-2
Structure of 146844-02-2 * Storage: {[proInfo.prStorage]}

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Product Details of [ 146844-02-2 ]

CAS No. :146844-02-2 MDL No. :MFCD00190908
Formula : C19H22ClNO4 Boiling Point : -
Linear Structure Formula :- InChI Key :GRGJVECUQLAEDM-UNTBIKODSA-N
M.W : 363.84 Pubchem ID :45789900
Synonyms :
Chemical Name :(R)-Dibenzyl 2-aminopentanedioate hydrochloride

Calculated chemistry of [ 146844-02-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 25
Num. arom. heavy atoms : 12
Fraction Csp3 : 0.26
Num. rotatable bonds : 10
Num. H-bond acceptors : 5.0
Num. H-bond donors : 1.0
Molar Refractivity : 96.98
TPSA : 78.62 ?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) : -6.24 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 3.21
Log Po/w (WLOGP) : 3.08
Log Po/w (MLOGP) : 2.77
Log Po/w (SILICOS-IT) : 3.25
Consensus Log Po/w : 2.46

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.81
Solubility : 0.0559 mg/ml ; 0.000154 mol/l
Class : Soluble
Log S (Ali) : -4.53
Solubility : 0.0107 mg/ml ; 0.0000293 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -5.58
Solubility : 0.000966 mg/ml ; 0.00000265 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 2.0
Synthetic accessibility : 3.0

Safety of [ 146844-02-2 ]

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 [ 146844-02-2 ]

* 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 [ 146844-02-2 ]

[ 146844-02-2 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 15761-38-3 ]
  • [ 146844-02-2 ]
  • [ 59524-70-8 ]
  • 2
  • [ 2177-34-6 ]
  • [ 146844-02-2 ]
  • benzyl 1-(3-cyclohexyl-3-oxopropyl)-5-oxo-D-prolinate [ No CAS ]
YieldReaction ConditionsOperation in experiment
62% With triethylamine; In propan-1-ol; at 0 - 5℃; for 3.0h;Heating / reflux; Intermediate 1.4; benzyl l-(3-cyclohexyl-3-oxopropyl)-5-oxo-D- prolinate; In a flame-dried, nitrogen- flushed IL round bottom flask with magnetic stirrer, D-Dibenzyl glutamate hydrochloride (H-D-GIu(OBn)-OBn) (0.04mol, 14.6g) was dissolved in anhydrous 1-propanol (0.5L). To the resulting solution cooled by ice bath, triethylamine (0.15mol, 21ml) was added at stirring under nitrogen. The mixture was stirred for 10 min followed by addition of freshly prepared vinylcyclohexylketone (0.05 mol). The reaction mixture was stirred under nitrogen at 0-50C for 3h until reaction was complete (Control by LC-MS and NMR of concentrated aliquots).When the reaction was complete, the cooling was removed, reflux condenser attached to the flask, and the mixture was refluxed overnight in an oil bath. The yellow solution was concentrated, diluted with a mixture of chloroform-hexanes (1:1 v/v, 100ml), and filtered from white needles Of Et3NHCl. The filtrate was concentrated again giving 26.1 g of light yellow oil. Purification on 20Og of silica gel, EPO <DP n="61"/>eluent hexanes-EtOAc from 100:0 to 0:100, gave 8.85g (62percent) of pure benzyl l-(3- cyclohexyl-3-oxopropyl)-5-oxo-D-prolinate as clear oil, Rf 0.30 (hexanes-EtOAc 1:4). 1H NMR (400 MHz, CDCl3 ) delta 7.36 (m, 5H, Ph), 5.19 (d, IH, 12.0Hz, CH2Ph), 5.15 (d, IH, 12.0Hz, OCH2Ph), 4.33 (m, IH, CH-COOBn), 4.11 (m, IH, cyclohexyl CH-CO), 3.62 (m, IH, CH2-N), 3.37 (m, IH, CH2-N), 2.89 (m, IH, chain CH2-CO), 2.66 (m, IH, chain CH2-CO), 2.43 (m, IH, lactam ring CH2-CO), 2.30 (m, IH, lactam ring CH2-CO), 2.27 (m, IH, lactam ring H3) 2.02 (m, IH, lactam ring H3), 1.85-1.55 (m, 5H, cyclohexyl), 1.30-1.15 (m, 5H, cyclohexyl). 13C NMR (100 MHz, CDC13) delta 211.9 (CO-C6Hn), 175.0 (-CO-N), 171.7 (COOBn), 135.0 (ipso-C Ph), 128.5, 128.2 (o-C, m-C Ph), 128.4 (p-C Ph), 67.5 (OCH2-Ph), 61.7 (CH-COOBn), 51.2 (cyclohexyl CH-CO), 39.2 (chain CH2CO), 38.2 (CH2-N), 30.1 (lactam ring CH2-CO), 29.0, 26.5, 26.3 (cyclohexyl), 24.1 (lactam ring C3).
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