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[ CAS No. 53525-65-8 ] {[proInfo.proName]}

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Chemical Structure| 53525-65-8
Chemical Structure| 53525-65-8
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Product Details of [ 53525-65-8 ]

CAS No. :53525-65-8 MDL No. :MFCD01631199
Formula : C8H4N4O2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :UYAAVKFHBMJOJZ-UHFFFAOYSA-N
M.W : 188.14 Pubchem ID :1051510
Synonyms :

Calculated chemistry of [ 53525-65-8 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 14
Num. arom. heavy atoms : 12
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 4.0
Num. H-bond donors : 0.0
Molar Refractivity : 47.67
TPSA : 68.74 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -7.5 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.64
Log Po/w (XLOGP3) : -0.07
Log Po/w (WLOGP) : -0.86
Log Po/w (MLOGP) : -0.34
Log Po/w (SILICOS-IT) : -0.26
Consensus Log Po/w : -0.18

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -1.6
Solubility : 4.76 mg/ml ; 0.0253 mol/l
Class : Very soluble
Log S (Ali) : -0.92
Solubility : 22.5 mg/ml ; 0.12 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.58
Solubility : 4.91 mg/ml ; 0.0261 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.13

Safety of [ 53525-65-8 ]

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

Application In Synthesis of [ 53525-65-8 ]

* 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 [ 53525-65-8 ]
  • Downstream synthetic route of [ 53525-65-8 ]

[ 53525-65-8 ] Synthesis Path-Upstream   1~6

  • 1
  • [ 1072-84-0 ]
  • [ 53525-65-8 ]
YieldReaction ConditionsOperation in experiment
95% for 18 h; Reflux The imidazole-2-carboxylic acid (5 g, 44.6 mmol) in suspensionin thionyl chloride (75 mL) was heated to reflux under agitation for18 h. The reaction mixture was cooled, then filtered, washed withtoluene, and dried under high vacuum. The compound is obtainedas a yellow solid (95percent yield). C8H4N4O2. MW: 188.14 g/mol. Mp265-268 °C. 1H NMR δ (ppm, 300 MHz, DMSO-d6) 8.24 (d, 1H,CHC-CO), 8.32 (d, 1H, CHC-CO, J3 Hz), 8.88 (d, 1H, CHN),9.28 (d, 1H, CHN, J3 Hz). 13C NMR δ (ppm, 100 MHz, DMSO-d6)123.99, 124.52, 125.62, 137.26, 139.73, 150.39, 159.68. MS (ESI+ ,QTof, m/z): 189.0 [M+H]+.
Reference: [1] Bioorganic and Medicinal Chemistry, 2008, vol. 16, # 13, p. 6601 - 6610
[2] European Journal of Medicinal Chemistry, 2017, vol. 138, p. 909 - 919
[3] Pharmaceutical Chemistry Journal, 1986, vol. 20, # 7, p. 460 - 463[4] Khimiko-Farmatsevticheskii Zhurnal, 1986, vol. 20, # 7, p. 799 - 802
[5] Patent: EP1439169, 2004, A1, . Location in patent: Page 81-82
  • 2
  • [ 1072-84-0 ]
  • [ 53525-65-8 ]
Reference: [1] Journal of Medicinal Chemistry, 2003, vol. 46, # 4, p. 457 - 460
  • 3
  • [ 17325-26-7 ]
  • [ 53525-65-8 ]
Reference: [1] Journal of Organic Chemistry, 1986, vol. 51, # 3, p. 306 - 309
  • 4
  • [ 13189-13-4 ]
  • [ 53525-65-8 ]
Reference: [1] Journal of Organic Chemistry, 1986, vol. 51, # 3, p. 306 - 309
  • 5
  • [ 56460-32-3 ]
  • [ 53525-65-8 ]
Reference: [1] Tetrahedron Letters, 2001, vol. 42, # 26, p. 4297 - 4299
  • 6
  • [ 61985-23-7 ]
  • [ 53525-65-8 ]
  • [ 79711-73-2 ]
  • [ 99560-60-8 ]
Reference: [1] Journal of Organic Chemistry, 1986, vol. 51, # 3, p. 306 - 309
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