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[ CAS No. 5462-30-6 ] {[proInfo.proName]}

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Chemical Structure| 5462-30-6
Chemical Structure| 5462-30-6
Structure of 5462-30-6 * Storage: {[proInfo.prStorage]}

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Product Details of [ 5462-30-6 ]

CAS No. :5462-30-6 MDL No. :MFCD00024301
Formula : C8H6Cl2N2O3 Boiling Point : -
Linear Structure Formula :- InChI Key :ZEGRPTYRAGSSBH-UHFFFAOYSA-N
M.W : 249.05 Pubchem ID :226498
Synonyms :

Calculated chemistry of [ 5462-30-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 15
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.12
Num. rotatable bonds : 3
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 59.6
TPSA : 74.92 ?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) : -6.11 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.75
Log Po/w (XLOGP3) : 2.41
Log Po/w (WLOGP) : 2.67
Log Po/w (MLOGP) : 1.59
Log Po/w (SILICOS-IT) : 0.57
Consensus Log Po/w : 1.8

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.0
Solubility : 0.249 mg/ml ; 0.000999 mol/l
Class : Soluble
Log S (Ali) : -3.63
Solubility : 0.059 mg/ml ; 0.000237 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.4
Solubility : 0.0985 mg/ml ; 0.000395 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.22

Safety of [ 5462-30-6 ]

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

Application In Synthesis of [ 5462-30-6 ]

* 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 [ 5462-30-6 ]

[ 5462-30-6 ] Synthesis Path-Upstream   1~5

  • 1
  • [ 2150-93-8 ]
  • [ 5462-30-6 ]
YieldReaction ConditionsOperation in experiment
95.23% at 3 - 13℃; for 6.5 h; 3,4-Dichloroacetanilide (II) (150 g, 0.74 moles) was slowly added to a reactor containing sulfuric acid (270 g, 99percent, 2.7 moles) at 13 °C, followed by stirring for 0.5 hours and then cooling to 8 °C. To this, oleum (422 g, 31.1percent, 4.61 moles) was added slowly, to obtain a mixture. The mixture comprised resultant sulfuric acid having strength of 104percent. The molar ratio of 3,4-dichloroacetanilide (II) and the resultant sulfuric acid in the mixture was 1: 10. The mixture was further cooled to 3 °C, and nitric acid (51 g, 98percent, 0.79 moles) was slowly added to the mixture over 5 hours. The resultant mixture was further stirred and the progress of the reaction was monitored by thin layer chromatography (TLC). 3,4-Dichloroacetanilide was completely consumed within 1 hour and a product mixture was obtained. The product mixture was carefully poured over 1650 g ice in 200 ml water while maintaining the temperature below 15 °C, followed by stirring for 15 min to obtain a dispersion. The dispersion was filtered to obtain a residue comprising 2-nitro-4,5-dichloroacetanilide (I). The residue was washed with water till it was free of residual acid, and the washed residue was dried to obtain 2-nitro-4,5-dichloroacetanilide (I) (174 g, yield = 95.23percent, HPLC purity = 97.83percent). (0069) HPLC analysis of the product showed the presence of 1.46percent III.
Reference: [1] Patent: WO2018/91978, 2018, A1, . Location in patent: Page/Page column 7-8
[2] Journal of Medicinal Chemistry, 1995, vol. 38, # 10, p. 1786 - 1792
  • 2
  • [ 2150-93-8 ]
  • [ 5462-30-6 ]
YieldReaction ConditionsOperation in experiment
92% at 3 - 13℃; for 6.5 h; Experiment 3: 3,4-Dichloroacetanilide (II) (150 g, 0.735 moles), sulfuric acid (156.0 g, 99percent w/w, 1.576 moles), oleum (260.5 g, 31.1percent w/w, 2.844 moles), and nitric acid (51 g, 98percent w/w, 0.79 moles) were used. The mixture comprised resultant sulfuric acid having strength of 104percent. The molar ratio of 3,4-Dichloroacetanilide (II) to the resultant sulfuric acid in the mixture was 1:6. The reaction conditions, and product yield and purity are summarized in Table 1. (0074) 177 g of 2-nitro-4,5-dichloroacetanilide (I) was obtained (yield = 92percent and HPLC purity of 92percent). HPLC analysis of product showed the presence of 6percent of III. 3,4-Dichloroacetanilide (II) (150 g, 0.74 moles) was slowly added to a reactor containing sulfuric acid (270 g, 99percent, 2.7 moles) at 13 °C, followed by stirring for 0.5 hours and then cooling to 8 °C. To this, oleum (422 g, 31.1percent, 4.61 moles) was added slowly, to obtain a mixture. The mixture comprised resultant sulfuric acid having strength of 104percent. The molar ratio of 3,4-dichloroacetanilide (II) and the resultant sulfuric acid in the mixture was 1: 10. The mixture was further cooled to 3 °C, and nitric acid (51 g, 98percent, 0.79 moles) was slowly added to the mixture over 5 hours. The resultant mixture was further stirred and the progress of the reaction was monitored by thin layer chromatography (TLC). 3,4-Dichloroacetanilide was completely consumed within 1 hour and a product mixture was obtained. The product mixture was carefully poured over 1650 g ice in 200 ml water while maintaining the temperature below 15 °C, followed by stirring for 15 min to obtain a dispersion. The dispersion was filtered to obtain a residue comprising 2-nitro-4,5-dichloroacetanilide (I). The residue was washed with water till it was free of residual acid, and the washed residue was dried to obtain 2-nitro-4,5-dichloroacetanilide (I) (174 g, yield = 95.23percent, HPLC purity = 97.83percent). (0069) HPLC analysis of the product showed the presence of 1.46percent III.
Reference: [1] Patent: WO2018/91978, 2018, A1, . Location in patent: Page/Page column 7-8; 9
  • 3
  • [ 95-76-1 ]
  • [ 5462-30-6 ]
Reference: [1] Journal of Medicinal Chemistry, 1995, vol. 38, # 10, p. 1786 - 1792
  • 4
  • [ 625-58-1 ]
  • [ 2150-93-8 ]
  • [ 5462-30-6 ]
Reference: [1] Journal of Organic Chemistry, 1954, vol. 19, p. 31,34, 35
  • 5
  • [ 108-24-7 ]
  • [ 95-76-1 ]
  • [ 5462-30-6 ]
Reference: [1] Gazzetta Chimica Italiana, 1977, vol. 107, p. 175 - 180
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