Home Cart 0 Sign in  

[ CAS No. 56502-01-3 ] {[proInfo.proName]}

,{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]}
Chemical Structure| 56502-01-3
Chemical Structure| 56502-01-3
Structure of 56502-01-3 * Storage: {[proInfo.prStorage]}
Cart0 Add to My Favorites Add to My Favorites Bulk Inquiry Inquiry Add To Cart

Quality Control of [ 56502-01-3 ]

Related Doc. of [ 56502-01-3 ]

Alternatived Products of [ 56502-01-3 ]

Product Details of [ 56502-01-3 ]

CAS No. :56502-01-3 MDL No. :MFCD01862939
Formula : C11H19NO4 Boiling Point : -
Linear Structure Formula :- InChI Key :GDWKIRLZWQQMIE-QMMMGPOBSA-N
M.W : 229.27 Pubchem ID :688605
Synonyms :

Calculated chemistry of [ 56502-01-3 ]

Physicochemical Properties

Num. heavy atoms : 16
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.82
Num. rotatable bonds : 5
Num. H-bond acceptors : 4.0
Num. H-bond donors : 1.0
Molar Refractivity : 63.17
TPSA : 66.84 Ų

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) : -6.87 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.31
Log Po/w (XLOGP3) : 1.16
Log Po/w (WLOGP) : 1.48
Log Po/w (MLOGP) : 1.03
Log Po/w (SILICOS-IT) : 0.6
Consensus Log Po/w : 1.32

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 0.0
Bioavailability Score : 0.56

Water Solubility

Log S (ESOL) : -1.66
Solubility : 4.99 mg/ml ; 0.0218 mol/l
Class : Very soluble
Log S (Ali) : -2.16
Solubility : 1.59 mg/ml ; 0.00694 mol/l
Class : Soluble
Log S (SILICOS-IT) : -0.78
Solubility : 38.0 mg/ml ; 0.166 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.75

Safety of [ 56502-01-3 ]

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

Application In Synthesis of [ 56502-01-3 ]

* 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 [ 56502-01-3 ]
  • Downstream synthetic route of [ 56502-01-3 ]

[ 56502-01-3 ] Synthesis Path-Upstream   1~10

  • 1
  • [ 88790-37-8 ]
  • [ 56502-01-3 ]
YieldReaction ConditionsOperation in experiment
92.6%
Stage #1: With sodium hydroxide; water In methanol
tert-Butyl (2S)-2-(2-methoxy-2-oxoethyl)-1-pyrrolidinecarboxylate (8.35 g, 34.3 mmol) was dissolved in 150 mL MeOH. Aqueous NaOH (50 mL, 1 M) was added and the reaction mixture was allowed to stand overnight. After concentration in vacuo to ca. 100 mL, the solution was added to 300 mL water and extracted with ether (2x). The carboxylate solution was acidified to pH 2 with 12 N HC1 and extracted with ether (2x). The aqueous layer was saturated with salt and extracted a third time with ether. The combined organic layers were washed with water, brine and dried over MgS04. Filtration and concentration provided the title acid as a white solid (7.28 g, 31.7 mmol, 92.6percent) :'H NMR (300 MHz, CDC13, mixture of rotamers) 6 4.16 (bs, 1H), 3.37 (bs, 2H), 3.0-2. 8 (bs, 1H), 2.36 (dd, J = 9.3, 15.3 Hz, 1H), 2.2-2. 0 (m, 1H), 1.9-1. 7 (m, 4H), 1.48 (s, 9H) ppm.
Reference: [1] Patent: WO2003/76440, 2003, A1, . Location in patent: Page/Page column 140
[2] Journal of Organic Chemistry, 2005, vol. 70, # 22, p. 8730 - 8733
[3] Organic and Biomolecular Chemistry, 2003, vol. 1, # 22, p. 3977 - 3988
[4] Tetrahedron Letters, 1997, vol. 38, # 20, p. 3609 - 3610
  • 2
  • [ 88790-38-9 ]
  • [ 56502-01-3 ]
YieldReaction ConditionsOperation in experiment
75%
Stage #1: With water; sodium hydroxide In methanol at 100℃; for 3 h;
Stage #2: With hydrogenchloride In methanol; water
Intermediate 4(S)-2-( 1 -(tert-Butoxycarbonyl)pyrrolidin-2-yl)acetic acid[0229][Chemical Formula 35]To a solution of intermediate 5 (35.2 g, 167 mmol) in methanol (167 mL) was added aqueous sodium hydroxide solution (30percentw/v, 167 mL), and heated to 100°C. After stirring for 3 hours, the reaction solution was concentrated under reduced pressure. To the obtained residue was added aqueous hydrochloric acid solution to adjust pH 4-5, and the aqueous layer was extracted with ethyl acetate. The organic layer was washed with water and brine, and then dried over sodium sulfate, and concentrated under reduced pressure to give the title compound (28.8 g, 125 mmol, 75percent).MS (ESI+) 230 (M++l, 100percent)
Reference: [1] Patent: WO2011/111875, 2011, A1, . Location in patent: Page/Page column 63
  • 3
  • [ 101130-03-4 ]
  • [ 56502-01-3 ]
Reference: [1] Journal of the Chemical Society. Perkin Transactions 1, 2002, # 18, p. 2087 - 2089
[2] Helvetica Chimica Acta, 1999, vol. 82, # 10, p. 1539 - 1558
[3] Tetrahedron Letters, 1997, vol. 38, # 20, p. 3609 - 3610
[4] RSC Advances, 2014, vol. 4, # 70, p. 37419 - 37422
  • 4
  • [ 24424-99-5 ]
  • [ 56502-01-3 ]
Reference: [1] Journal of Medicinal Chemistry, 2002, vol. 45, # 12, p. 2571 - 2578
  • 5
  • [ 24424-99-5 ]
  • [ 56633-75-1 ]
  • [ 56502-01-3 ]
Reference: [1] Bioorganic and Medicinal Chemistry Letters, 1996, vol. 6, # 4, p. 361 - 366
[2] Chemistry - An Asian Journal, 2014, vol. 9, # 4, p. 1060 - 1067
  • 6
  • [ 15761-39-4 ]
  • [ 56502-01-3 ]
Reference: [1] Tetrahedron Letters, 1997, vol. 38, # 20, p. 3609 - 3610
[2] RSC Advances, 2014, vol. 4, # 70, p. 37419 - 37422
  • 7
  • [ 118758-56-8 ]
  • [ 56502-01-3 ]
  • [ 101555-60-6 ]
Reference: [1] Tetrahedron Asymmetry, 2004, vol. 15, # 21, p. 3407 - 3412
  • 8
  • [ 141874-26-2 ]
  • [ 56502-01-3 ]
Reference: [1] Tetrahedron Letters, 1997, vol. 38, # 20, p. 3609 - 3610
  • 9
  • [ 186581-53-3 ]
  • [ 15761-39-4 ]
  • [ 56502-01-3 ]
Reference: [1] Organic Syntheses, 2002, vol. 79, p. 154 - 154
  • 10
  • [ 118758-56-8 ]
  • [ 56502-01-3 ]
  • [ 101555-60-6 ]
Reference: [1] Tetrahedron Asymmetry, 2004, vol. 15, # 21, p. 3407 - 3412
Same Skeleton Products
Historical Records

Related Functional Groups of
[ 56502-01-3 ]

Amino Acid Derivatives

Chemical Structure| 1159983-30-8

[ 1159983-30-8 ]

2-(4-Amino-1-(tert-butoxycarbonyl)piperidin-4-yl)acetic acid

Similarity: 0.90

Chemical Structure| 887587-09-9

[ 887587-09-9 ]

1-(tert-Butoxycarbonyl)-3-methylpyrrolidine-3-carboxylic acid

Similarity: 0.88

Chemical Structure| 59378-75-5

[ 59378-75-5 ]

1-(tert-Butoxycarbonyl)pyrrolidine-3-carboxylic acid

Similarity: 0.88

Chemical Structure| 72925-16-7

[ 72925-16-7 ]

(R)-1-(tert-Butoxycarbonyl)pyrrolidine-3-carboxylic acid

Similarity: 0.88

Chemical Structure| 140148-70-5

[ 140148-70-5 ]

(S)-1-Boc-Pyrrolidine-3-carboxylic acid

Similarity: 0.88