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[ CAS No. 31963-35-6 ] {[proInfo.proName]}

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Chemical Structure| 31963-35-6
Chemical Structure| 31963-35-6
Structure of 31963-35-6 * Storage: {[proInfo.prStorage]}
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Product Details of [ 31963-35-6 ]

CAS No. :31963-35-6 MDL No. :MFCD08271962
Formula : C13H14ClNO Boiling Point : -
Linear Structure Formula :- InChI Key :USRYZTSPSJXQFU-UHFFFAOYSA-N
M.W : 235.71 Pubchem ID :17749840
Synonyms :

Calculated chemistry of [ 31963-35-6 ]

Physicochemical Properties

Num. heavy atoms : 16
Num. arom. heavy atoms : 12
Fraction Csp3 : 0.08
Num. rotatable bonds : 3
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 67.6
TPSA : 35.25 Ų

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.53 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 3.11
Log Po/w (WLOGP) : 3.59
Log Po/w (MLOGP) : 2.95
Log Po/w (SILICOS-IT) : 2.68
Consensus Log Po/w : 2.46

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.62
Solubility : 0.0568 mg/ml ; 0.000241 mol/l
Class : Soluble
Log S (Ali) : -3.52
Solubility : 0.0714 mg/ml ; 0.000303 mol/l
Class : Soluble
Log S (SILICOS-IT) : -4.71
Solubility : 0.00465 mg/ml ; 0.0000197 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.73

Safety of [ 31963-35-6 ]

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 [ 31963-35-6 ]

* 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.

  • Downstream synthetic route of [ 31963-35-6 ]

[ 31963-35-6 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 107624-14-6 ]
  • [ 31963-35-6 ]
YieldReaction ConditionsOperation in experiment
With hydrogenchloride; In diethyl ether; for 2.0h; A solution of 2-phenoxybenzonitrile (from step (ii) above (10.1 g, 0.0517 mol) in THF (50 ml) was added dropwise to the well-stirred suspension of LAH (4.9 g, 0.129 mol) in THF (50 ml) at 0 C. under nitrogen atmosphere and then allowed to stir at room temperature for overnight. The reaction mixture was quenched with 6(N) KOH (5 ml) 0 C. and stirred with THF (50 ml) for another 30 minutes. The reaction mixture was filtered and the residue was washed with ethyl acetate. The filtrate was concentrated to give the crude amine. Satd. HCl in diethyl ether (20 ml) was added to the solution of crude amine in diethyl ether (20 ml) and stirred for 2 h. Then the reaction mixture was filtered and residue was dried to give the title compound (10 g, 97.08
  • 2
  • [ 1028338-59-1 ]
  • [ 31963-35-6 ]
  • [ 1028336-90-4 ]
YieldReaction ConditionsOperation in experiment
37.0% With sodium t-butanolate;tris-(dibenzylideneacetone)dipalladium(0); 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; In ISOPROPYLAMIDE; at 80.0℃; for 1.0h; Example 95: 4-Chloro-6-(2-phenoxy-benzyIamino)-2H-phthalazin-l-one; A mixture 6-bromo-4-chloro-2H-phthalazin-l-one (150 mg, 0.58 mmol), 2- phenoxy-benzylamine hydrochloride (151 mg, 0.64 mmol), Pd2(dba)3 (53 mg, 0.058 mmol), rac-BINAP (132 mg, 0.17 mmol) and NaOt-Bu (200 mg, 2.1 mmol) in DMA (6 mL) was heated at 8O0C for Ih. The mixture was allowed to cool, diluted with EtOAc (25 mL) and washed with water (25 mL). The organic layer was dried over anhydrous sodium sulfate and concentrated. Chromatography on silica (EtOAc/hexanes) yielded the title compound. 4-Chloro-6-(2-phenoxy-benzylamino)-2H-phthalazin-l-one: 81 mg (37.0%): m/z (M+eta)=378. 1H-NMR (DMSO-J5) delta: 12.77 (s,lH), 8.34 (d,lH), 8.03(m,lH), 7.82 (m,3H), 7.71 (m,lH), 7.56 (m,3H), 7.42 (m,2H), 7.33 (dd,lH), 7.20 (s,lH), 4.84 (d,2H).
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