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[ CAS No. 284493-67-0 ] {[proInfo.proName]}

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Chemical Structure| 284493-67-0
Chemical Structure| 284493-67-0
Structure of 284493-67-0 * Storage: {[proInfo.prStorage]}
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Product Details of [ 284493-67-0 ]

CAS No. :284493-67-0 MDL No. :MFCD02090710
Formula : C14H18ClNO4 Boiling Point : -
Linear Structure Formula :- InChI Key :UDUKZORPLJUWTF-UHFFFAOYSA-N
M.W : 299.75 Pubchem ID :4404164
Synonyms :

Calculated chemistry of [ 284493-67-0 ]

Physicochemical Properties

Num. heavy atoms : 20
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.43
Num. rotatable bonds : 7
Num. H-bond acceptors : 4.0
Num. H-bond donors : 2.0
Molar Refractivity : 76.35
TPSA : 75.63 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) : -6.3 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.38
Log Po/w (XLOGP3) : 2.58
Log Po/w (WLOGP) : 3.06
Log Po/w (MLOGP) : 2.49
Log Po/w (SILICOS-IT) : 2.3
Consensus Log Po/w : 2.56

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.08
Solubility : 0.247 mg/ml ; 0.000824 mol/l
Class : Soluble
Log S (Ali) : -3.82
Solubility : 0.0457 mg/ml ; 0.000153 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.78
Solubility : 0.0496 mg/ml ; 0.000166 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 2.72

Safety of [ 284493-67-0 ]

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 [ 284493-67-0 ]

* 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.

  • Downstream synthetic route of [ 284493-67-0 ]

[ 284493-67-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 284493-67-0 ]
  • [ 942316-88-3 ]
  • [2-{(S)-1-[5-chloro-4-(4-hydroxy-2-oxo-1,2-dihydroquinolin-6-yl)-1H-imidazol-2-yl]-2-phenylethylcarbamoyl}-1-(3-chlorophenyl)ethyl]carbamic acid tert-butyl ester [ No CAS ]
YieldReaction ConditionsOperation in experiment
With benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20℃; 109 [2-{(S)-l-[5-Chloro-4-(4-hydroxy-2-oxo-l,2-dihydro-quinolin-6-yl)-lH-imidazol- 2-yl]-2-phenyl-ethylcarbamoyl}-l-(3-chloro-phenyl)-ethyl]-carbamic acid tert- butyl ester, trifluoroacetic acid salt[00360] To a solution of 65G (50 mg, 0.131 mmol) in DMF (1.5 mL) were added 3-(tert-butoxycarbonylamino)-3-(3-chlorophenyl)propanoic acid (50 mg, 0.167 mmol), PyBOP (100 mg, 0.192 mmol) and DIEA (0.1 ml, 0.573 mmol), and the reaction mixture was stirred under nitrogen at rt overnight. The crude product was diluted with methanol and purified by prep ηPLC to give 109 (24mg, 23.54%).LCMS m/z 662.36 (M+η)+. 1HNMR (400 MHz, CD3OD, two diastereomers) δ: 1.35(d, J=9.67 Hz, 9 H), 2.47 - 2.73 (m, 2 H), 3.02 - 3.25 (m, 2 H), 4.81 - 5.04 (m, 1 H)3 5.15 (t, J=7.91 Hz, 1 H), 5.96 (s, 1 H), 7.02 - 7.34 (m, 8 H), 7.41 (dd, J=8.79, 2.20 Hz, 1 H), 7.85 (ddd, /=8.68, 2.09, 1.98 Hz, 1 H), 8.15 - 8.31 (m, 1 H).
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