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[ CAS No. 84955-31-7 ] {[proInfo.proName]}

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Chemical Structure| 84955-31-7
Chemical Structure| 84955-31-7
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Product Details of [ 84955-31-7 ]

CAS No. :84955-31-7 MDL No. :MFCD07369229
Formula : C6H5ClN4 Boiling Point : No data available
Linear Structure Formula :- InChI Key :VIVLSUIQHWGALQ-UHFFFAOYSA-N
M.W : 168.58 Pubchem ID :5324413
Synonyms :

Calculated chemistry of [ 84955-31-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 2.0
Num. H-bond donors : 2.0
Molar Refractivity : 43.3
TPSA : 67.59 ?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) : -6.42 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.21
Log Po/w (XLOGP3) : 1.28
Log Po/w (WLOGP) : 1.2
Log Po/w (MLOGP) : 0.6
Log Po/w (SILICOS-IT) : 1.49
Consensus Log Po/w : 1.16

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.3
Solubility : 0.851 mg/ml ; 0.00505 mol/l
Class : Soluble
Log S (Ali) : -2.3
Solubility : 0.847 mg/ml ; 0.00503 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.79
Solubility : 0.274 mg/ml ; 0.00163 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.59

Safety of [ 84955-31-7 ]

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

Application In Synthesis of [ 84955-31-7 ]

* 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 [ 84955-31-7 ]
  • Downstream synthetic route of [ 84955-31-7 ]

[ 84955-31-7 ] Synthesis Path-Upstream   1~2

  • 1
  • [ 84955-31-7 ]
  • [ 86392-75-8 ]
Reference: [1] Journal of Heterocyclic Chemistry, 1988, vol. 25, # 6, p. 1893 - 1898
[2] Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1988, p. 697 - 702
[3] Tetrahedron Letters, 1987, vol. 28, # 43, p. 5107 - 5110
[4] Tetrahedron Letters, 1987, vol. 28, # 43, p. 5107 - 5110
  • 2
  • [ 84955-31-7 ]
  • [ 93366-88-2 ]
YieldReaction ConditionsOperation in experiment
90% With ammonia In methanol; water for 17 h; To a suspension of 2-AMINO-4- CHLORO-7H-PYRROLO [2, 3-d] pyrimidine (1) (1.0 g, 6.0 mmol) in MeOH (50 mL) and aqueous ammonium hydroxide (1 mL) was added 10percent Pd-C (500 mg). The reaction mixture was stirred under atmospheric pressure for 17 h and the catalyst was filtered through A pad of Celite. The filtrate was concentrated and chromatographed with silica gel (CH2CL2 : MEOH = 90: 10) to yield 717 mg of the target compound (90percent). H NMR (DMSO-D6) : 8 11.4 (bs, 1H), 8. 50 (s, 1 H), 7.11 (dd, J= 3. 6,0. 6 HZ, 1H), 6.49 (bs, 2H), 6.32 (dd, J= 3. 6,0. 9 HZ, 1 H).
Reference: [1] Bioorganic and Medicinal Chemistry Letters, 2007, vol. 17, # 18, p. 5261 - 5264
[2] Patent: WO2004/80466, 2004, A1, . Location in patent: Page/Page column 32
[3] Liebigs Annalen der Chemie, 1984, # 10, p. 1719 - 1730
[4] Bioorganic and Medicinal Chemistry Letters, 2010, vol. 20, # 1, p. 334 - 337
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