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[ CAS No. 156478-71-6 ] {[proInfo.proName]}

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Chemical Structure| 156478-71-6
Chemical Structure| 156478-71-6
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Product Details of [ 156478-71-6 ]

CAS No. :156478-71-6 MDL No. :MFCD02682402
Formula : C11H20N2O4 Boiling Point : -
Linear Structure Formula :- InChI Key :WZBHMXRBXXCEDD-UHFFFAOYSA-N
M.W : 244.29 Pubchem ID :2735642
Synonyms :
Chemical Name :2-(4-(tert-Butoxycarbonyl)piperazin-1-yl)acetic acid

Calculated chemistry of [ 156478-71-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 17
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.82
Num. rotatable bonds : 5
Num. H-bond acceptors : 5.0
Num. H-bond donors : 1.0
Molar Refractivity : 69.98
TPSA : 70.08 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -9.04 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.23
Log Po/w (XLOGP3) : -1.76
Log Po/w (WLOGP) : -0.14
Log Po/w (MLOGP) : 0.22
Log Po/w (SILICOS-IT) : -0.2
Consensus Log Po/w : 0.07

Druglikeness

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

Water Solubility

Log S (ESOL) : 0.08
Solubility : 297.0 mg/ml ; 1.21 mol/l
Class : Highly soluble
Log S (Ali) : 0.8
Solubility : 1550.0 mg/ml ; 6.36 mol/l
Class : Highly soluble
Log S (SILICOS-IT) : -0.35
Solubility : 110.0 mg/ml ; 0.45 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.41

Safety of [ 156478-71-6 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P280-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H332-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 156478-71-6 ]

* 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.

  • Downstream synthetic route of [ 156478-71-6 ]

[ 156478-71-6 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 280-13-7 ]
  • [ 156478-71-6 ]
  • [ 666852-94-4 ]
YieldReaction ConditionsOperation in experiment
With benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; N-ethyl-N,N-diisopropylamine; In dichloromethane; for 16h; EDC (1.18g, 6.15 mmol) was added to a stirred solution of [N-BOC-PIPERAZINE] acetic acid [(L.] [OOG,] 4.10 mmol), 8-oxa-3-aza-bicyclo [3.2. 1. ] octane (0.556g, 4.92 mmol), 3-hydroxy benzotriazole (0.836g, 6.15 mmol), and diisopropylethylamine (2. 14ml, 12.31 mmol) in DCM (20 ml) at ambient temperature under nitrogen. After stirring for 16h the reaction was quenched by the addition of water [(20ML).] The phases were separated and the organics were washed with sat. brine [(20ML),] dried and evaporated to dryness under reduced pressure. The residue was purified by chromatography on silica, eluting with 0-10% MeOH/DCM to give 46 as a white solid (0.780g). MS-ESI: 340 (M++H). [1H NMR (CDC13)] 1.45 (s, 9H), 1.80-2. 00 (m, 4H), 2.30-2. 58 (m, 4H), 2.85-3. 04 (m, [2H),] 3.25 (d, 1H), 3.30-3. 57 (m, 3H), 3.78 (d, 1H), 4.12 (d, 1H), 4.36 (d, 3H).
  • 2
  • [ 156478-71-6 ]
  • [ 59702-07-7 ]
  • C16H28N4O4 [ No CAS ]
YieldReaction ConditionsOperation in experiment
With dmap; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; In dichloromethane; at 20℃; for 16h; A mixture [OF N-BOC-4-PIPERAZINE-ACETIC] acid hydrochloride dihydrate (0.4g, 1.26 mmol), N- methyl-2-piperazinone (0.194g, [1.] [7MMOL),] DMAP [(L.] [OG,] 8.2 mmol) and EDC (0.4g, 2. [1MMOL)] in dichloromethane (60 ml) was stirred under a nitrogen atmosphere for 16h. The reaction mixture was washed with a [L.] OM aq. citric acid solution (2 x 50ml), sat. sodium bicarbonate solution, the organics separated, dried and evaporated to dryness under reduced pressure. The residue was purified by chromatography on silica eluting with 10- 20percent MEOH/EtOAc to give 66 (0.3g) as a solid foam. MS-ESI: 341 [(M++H).] [1H NMR (DMSOD6)] 1.50 (s, 9H), 2.48 (m, 4H), 2.97 (s, 3H), 3.22-3. 56 (m, 8H), 3.78 3.90 (2t, 2H), 4.09 4.29 (2s, 2H).
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