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[ CAS No. 5750-76-5 ] {[proInfo.proName]}

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Chemical Structure| 5750-76-5
Chemical Structure| 5750-76-5
Structure of 5750-76-5 * Storage: {[proInfo.prStorage]}

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Product Details of [ 5750-76-5 ]

CAS No. :5750-76-5 MDL No. :MFCD03788200
Formula : C4HCl3N2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :GIKMWFAAEIACRF-UHFFFAOYSA-N
M.W : 183.42 Pubchem ID :237259
Synonyms :

Calculated chemistry of [ 5750-76-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 37.06
TPSA : 25.78 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.47 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.88
Log Po/w (XLOGP3) : 2.75
Log Po/w (WLOGP) : 2.44
Log Po/w (MLOGP) : 1.43
Log Po/w (SILICOS-IT) : 2.99
Consensus Log Po/w : 2.3

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 2.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -3.2
Solubility : 0.115 mg/ml ; 0.000627 mol/l
Class : Soluble
Log S (Ali) : -2.95
Solubility : 0.208 mg/ml ; 0.00113 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.5
Solubility : 0.0579 mg/ml ; 0.000316 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.68

Safety of [ 5750-76-5 ]

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

Application In Synthesis of [ 5750-76-5 ]

* 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 [ 5750-76-5 ]

[ 5750-76-5 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 5369-19-7 ]
  • [ 5750-76-5 ]
  • 2,5-dichloro-N<SUP>4</SUP>-(3-tert-butylphenyl)pyrimidin-4-amine [ No CAS ]
YieldReaction ConditionsOperation in experiment
96% With N-ethyl-N,N-diisopropylamine; In ethanol; for 14h;Reflux; 2,5-Dichloro-iV4-(3-teri-butylphenyl)pyrimidin-4-amine (SG1-175): A solution of 2,4,5-trichloropyrimidine (1.00 g), 3-(tert-butyl)aniline (0.813 mg), and DIPEA (5.70 mL) in EtOH (5 mL) was heated at reflux for 14 h. The mixture was concentrated under reduced pressure. The residue was dissolved in EtOAc (50 mL) and washed with water (2 x 50 mL) and brine (50 mL). The organic layer was dried (Na2S04) and concentrated under reduced pressure to give the title compound as a brown solid (1.545 g, 96percent). Mp: 107-110 °C. NMR (400 MHz, DMSO-i): delta 9.48 (s, 1H, disappeared on D2O shake), 8.35 (s, 1H), 7.62 (t, J= 1.9 Hz, 1H), 7.41 (ddd, J= 7.8, 1.9, 1.0 Hz, 1H), 7.29 (t, J = 7.8 Hz, 1H), 7.19 (ddd, J= 7.8, 1.9, 1.0 Hz, 1H), 1.27 (s, 9H). HPLC-MS (ESI+): m/z 300.1 [10percent, (M37C137C1+H)+], 298.1 [65percent, (M35C137C1+H)+], 296.1 [100percent, (M35C135C1+H)+].
96% With N-ethyl-N,N-diisopropylamine; In ethanol; for 14h;Reflux; A solution of 2,4,5-trichloropyrimidine (1.00 g), 3-(i<?ri-butyl)aniline (0.813 mg), and DIPEA (5.70 mL) in EtOH (5 mL) was heated at reflux for 14 h. The mixture was concentrated under reduced pressure. The residue was dissolved in EtOAc (50 mL) and washed with water (2 x 50 mL) and brine (50 mL). The organic layer was dried (Na2S04) and concentrated under reduced pressure to give the title compound as a brown solid (1.545 g, 96percent). Mp: 107-110 °C. NMR (400 MHz, DMSO-ifc): delta 9.48 (s, IH, disappeared on D20 shake), 8.35 (s, IH), 7.62 (t, / = 1.9 Hz, IH), 7.41 (ddd, J = 7.8, 1.9, 1.0 Hz, IH), 7.29 (t, / = 7.8 Hz, IH), 7.19 (ddd, / = 7.8, 1.9, 1.0 Hz, IH), 1.27 (s, 9H). HPLC-MS (ESI+): m/z 300.1 [10percent, (M37C137C1+H)+], 298.1 [65percent, (M35C137C1+H)+], 296.1 [100percent, (M35C135C1+H)+].
  • 2
  • [ 20876-36-2 ]
  • [ 5750-76-5 ]
  • 5-((2,5-cichloropyrimidin-4-yl)amino)indolin-2-one [ No CAS ]
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