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[ CAS No. 38202-27-6 ] {[proInfo.proName]}

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Chemical Structure| 38202-27-6
Chemical Structure| 38202-27-6
Structure of 38202-27-6 * Storage: {[proInfo.prStorage]}

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Product Details of [ 38202-27-6 ]

CAS No. :38202-27-6 MDL No. :MFCD00009244
Formula : C13H19NO4S Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 285.36 Pubchem ID :-
Synonyms :

Calculated chemistry of [ 38202-27-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 19
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.46
Num. rotatable bonds : 5
Num. H-bond acceptors : 5.0
Num. H-bond donors : 0.0
Molar Refractivity : 74.71
TPSA : 73.34 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.7 cm/s

Lipophilicity

Log Po/w (iLOGP) : 3.12
Log Po/w (XLOGP3) : 3.29
Log Po/w (WLOGP) : 3.77
Log Po/w (MLOGP) : 3.1
Log Po/w (SILICOS-IT) : 2.68
Consensus Log Po/w : 3.19

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.59
Solubility : 0.0741 mg/ml ; 0.00026 mol/l
Class : Soluble
Log S (Ali) : -4.51
Solubility : 0.00891 mg/ml ; 0.0000312 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -4.23
Solubility : 0.0167 mg/ml ; 0.0000585 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 3.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 3.27

Safety of [ 38202-27-6 ]

Signal Word:Danger Class:4.1
Precautionary Statements:P240-P210-P241-P264-P280-P302+P352-P370+P378-P337+P313-P305+P351+P338-P362+P364-P332+P313 UN#:1325
Hazard Statements:H315-H319-H228 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 38202-27-6 ]

* 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.

  • Upstream synthesis route of [ 38202-27-6 ]
  • Downstream synthetic route of [ 38202-27-6 ]

[ 38202-27-6 ] Synthesis Path-Upstream   1~2

  • 1
  • [ 108-89-4 ]
  • [ 38202-27-6 ]
  • [ 105-37-3 ]
  • [ 51135-70-7 ]
YieldReaction ConditionsOperation in experiment
2.73 g
Stage #1: With perchloric acid In tetrahydrofuran at 0℃; for 1.5 h;
Stage #2: at 0 - 35℃;
Stage #3: With potassium carbonate In N,N-dimethyl-formamide at 10 - 35℃;
To a solution of ethyl N-(mesitylsulfonyl)oxyacetoimidate (14.7 g) in THF (15 mL) was added 60percent perchloric acid (11.2 mL) at 0°, the mixture was stirred for 90 min, and to the reaction mixture was added ice water.
The insoluble substance was collected by filtration, washed with water, and dried under stream.
The residue was added to a solution of 4-methylpyridine (4.18 mL) in THF (80 mL) at 0° C., and the mixture was stirred overnight at room temperature.
The solvent was evaporated under reduced pressure, DMF (80 mL), ethyl propionate (5.21 mL) and potassium carbonate (11.9 g) were added thereto, and the mixture was stirred overnight at room temperature.
To the reaction mixture was added water, and the mixture was extracted with ethyl acetate.
The extract was washed with 1N hydrochloric acid and saturated brine, and dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure.
The residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (2.73 g).
1H NMR (300 MHz, CDCl3) δ 1.41 (3H, t, J=7.2 Hz), 2.47 (3H, s), 4.38 (2H, q, J=6.9 Hz), 6.77 (1H, dd, J=7.0, 1.7 Hz), 7.93 (1H, s), 8.34 (1H, s), 8.39 (1H, d, J=7.2 Hz).
Reference: [1] Patent: US2015/266872, 2015, A1, . Location in patent: Paragraph 0739; 0740
  • 2
  • [ 626-55-1 ]
  • [ 38202-27-6 ]
  • [ 55899-13-3 ]
Reference: [1] Patent: EP2669285, 2013, A1, . Location in patent: Paragraph 0423; 0424
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