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[ CAS No. 119020-03-0 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 119020-03-0
Chemical Structure| 119020-03-0
Structure of 119020-03-0 * Storage: {[proInfo.prStorage]}

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Product Details of [ 119020-03-0 ]

CAS No. :119020-03-0 MDL No. :MFCD06658394
Formula : C13H18N2O2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :NQGRCKNDDGCZPV-UHFFFAOYSA-N
M.W : 234.29 Pubchem ID :4712622
Synonyms :

Calculated chemistry of [ 119020-03-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 17
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.46
Num. rotatable bonds : 5
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 69.33
TPSA : 55.56 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.85 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.68
Log Po/w (XLOGP3) : 1.24
Log Po/w (WLOGP) : 1.21
Log Po/w (MLOGP) : 1.41
Log Po/w (SILICOS-IT) : 1.25
Consensus Log Po/w : 1.56

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.01
Solubility : 2.32 mg/ml ; 0.00989 mol/l
Class : Soluble
Log S (Ali) : -2.0
Solubility : 2.32 mg/ml ; 0.00989 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.76
Solubility : 0.408 mg/ml ; 0.00174 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.61

Safety of [ 119020-03-0 ]

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

Application In Synthesis of [ 119020-03-0 ]

* 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 [ 119020-03-0 ]
  • Downstream synthetic route of [ 119020-03-0 ]

[ 119020-03-0 ] Synthesis Path-Upstream   1~8

  • 1
  • [ 141774-67-6 ]
  • [ 119020-03-0 ]
YieldReaction ConditionsOperation in experiment
82% With water; triphenylphosphine In tetrahydrofuran at 20℃; for 12 h; General procedure: To a stirred soln of azide derivative 9a or 9b (4.03 mmol) in THF (1 mL) was added solid Ph3P (4.03 mmol) and H2O (6.04 mmol). The resulting solution was stirred for 12 h at r.t., then concentrated under reduced pressure. The crude product was purified by flash column chromatography on silica gel (MeOH–CH2Cl2, 9:1).
Reference: [1] Synthetic Communications, 2011, vol. 41, # 17, p. 2517 - 2523
[2] Synthesis (Germany), 2013, vol. 45, # 17, p. 2458 - 2468
[3] Tetrahedron Letters, 2010, vol. 51, # 1, p. 209 - 212
[4] Tetrahedron Letters, 1991, vol. 32, # 49, p. 7183 - 7186
  • 2
  • [ 34079-31-7 ]
  • [ 119020-03-0 ]
YieldReaction ConditionsOperation in experiment
74%
Stage #1: With borane In tetrahydrofuran at 0℃; for 7 h; Heating / reflux
Stage #2: With hydrogenchloride; water In tetrahydrofuran at 0℃; for 6 h; Heating / reflux
Stage #3: With sodium hydroxide In tetrahydrofuran; water
A typical procedure for the reduction is as follows: starting with a solution of (S)-2-carbamoyl-l-7V-CBz-pyrrolidine (0.5g, 2mmol) in THF (10ml), borane BH3 (12ml, 12mmol, 1 .OM THF solution) was added slowly at 0°C under N2. The resulting solution was heated to reflux for 7 hours, then cooled to 0°C, followed by slow addition of 4.5mL of 12N HC1 to destroy the B-N complex. The mixture was heated to reflux for 6 hours, cooled to roomed temperature (RT), then was neutralized to ph8 by a WNaOH aqueous solution. After THF and water were removed under reduced pressure, the crude product was purified by use offlash silica gel column chromatography (1/10 = MeOH/CHzC^) to afford a clear, slightlyyellow oil in 74percent yield (348mg).
Reference: [1] Chemistry - A European Journal, 2006, vol. 12, # 16, p. 4321 - 4332
[2] Patent: WO2006/7586, 2006, A1, . Location in patent: Page/Page column 31-32
  • 3
  • [ 63808-36-6 ]
  • [ 119020-03-0 ]
Reference: [1] Journal of Organic Chemistry, 2009, vol. 74, # 15, p. 5260 - 5266
  • 4
  • [ 6216-63-3 ]
  • [ 119020-03-0 ]
Reference: [1] Tetrahedron Letters, 1991, vol. 32, # 49, p. 7183 - 7186
[2] Synthetic Communications, 2011, vol. 41, # 17, p. 2517 - 2523
[3] Synthesis (Germany), 2013, vol. 45, # 17, p. 2458 - 2468
  • 5
  • [ 1148-11-4 ]
  • [ 119020-03-0 ]
Reference: [1] Tetrahedron Letters, 1991, vol. 32, # 49, p. 7183 - 7186
[2] Synthetic Communications, 2011, vol. 41, # 17, p. 2517 - 2523
[3] Synthesis (Germany), 2013, vol. 45, # 17, p. 2458 - 2468
  • 6
  • [ 72500-24-4 ]
  • [ 119020-03-0 ]
Reference: [1] Tetrahedron Letters, 1991, vol. 32, # 49, p. 7183 - 7186
[2] Synthetic Communications, 2011, vol. 41, # 17, p. 2517 - 2523
  • 7
  • [ 501-53-1 ]
  • [ 119020-03-0 ]
Reference: [1] Tetrahedron Letters, 1991, vol. 32, # 49, p. 7183 - 7186
  • 8
  • [ 147-85-3 ]
  • [ 119020-03-0 ]
Reference: [1] Tetrahedron Letters, 1991, vol. 32, # 49, p. 7183 - 7186
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