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[ CAS No. 197569-11-2 ]

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Chemical Structure| 197569-11-2
Chemical Structure| 197569-11-2
Structure of 197569-11-2 * Storage: {[proInfo.prStorage]}
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Product Details of [ 197569-11-2 ]

CAS No. :197569-11-2 MDL No. :MFCD03695496
Formula : C12H18N2O2 Boiling Point : -
Linear Structure Formula :- InChI Key :N/A
M.W :222.28 g/mol Pubchem ID :-
Synonyms :

Calculated chemistry of of [ 197569-11-2 ]

Physicochemical Properties

Num. heavy atoms : 16
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.67
Num. rotatable bonds : 3
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 65.48
TPSA : 53.33 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) : -6.78 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.74
Log Po/w (XLOGP3) : 1.24
Log Po/w (WLOGP) : 2.09
Log Po/w (MLOGP) : 1.23
Log Po/w (SILICOS-IT) : 1.54
Consensus Log Po/w : 1.77

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.8
Solubility : 3.51 mg/ml ; 0.0158 mol/l
Class : Very soluble
Log S (Ali) : -1.96
Solubility : 2.45 mg/ml ; 0.011 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.63
Solubility : 5.23 mg/ml ; 0.0236 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.79

Safety of [ 197569-11-2 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P280 UN#:N/A
Hazard Statements:H302-H312-H332 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 197569-11-2 ]

* 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 [ 197569-11-2 ]

[ 197569-11-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1629037-78-0 ]
  • [ 197569-11-2 ]
  • [ 1629072-94-1 ]
YieldReaction ConditionsOperation in experiment
With 1,8-diazabicyclo[5.4.0]undec-7-ene In acetonitrile at 20℃; for 72h; Inert atmosphere; 8 tert-butyl 4-(3-amino-4-(benzyloxy)-lH-pyrazolo[4,3-c]pyridin-l-yl)-4- (cyan omethyl)p ip er idine- 1 -car b oxylate To a solution of 4-(benzyloxy)-lH-pyrazolo[4,3-c]pyridin-3-amine (155 g, 645 mmol) in CH3CN (2.50 L), was added (batchwise) iert-butyl 4-(cyanomethylidene)piperidine-l- carboxylate (286 g, 1.29 mol) followed by dropwise addition of DBU (99.0 g, 650 mmol) at 20°C over 20 minutes. The resulting solution was stirred for 3 days at 20°C, concentrated in vacuo at 40-45°C, and then purified by silica chromatography, eluting with 0-50% ethyl acetate/petroleum ether. Concentration of the desired fraction in vacuo afforded compound 1-8. LRMS (ESI) calc'd for C25H3iN603 [M+H]+: 463, found 463. 1H NMR (300 MHz, CDC13): δ 7.82 (d, 1H), 7.34-7.50 (m, 5H), 6.84 (d, 1H), 5.54 (s, 2H), 4.51 (br s, 2H), 3.94-3.97 (d, 2H), 3.05 (br s, 2H), 2.85-2.90 (m, 2H), 2.79 (s, 2H), 1.92-2.04 (m, 2H), 1.45 (s, 9H).
With 1,8-diazabicyclo[5.4.0]undec-7-ene In acetonitrile at 20℃; Inert atmosphere; 1 Step 1: tert-butyl 4-’(3--amino-’4--( benzyloxy)-’iiipyrazolo[4,3--c1pyridin--i--yfl--4-- (cyanomethyl )piperidine- I -carboxylate To a solution of 4-.(henzyioxy-’1iI-pyrazoio[4,3--c]pyridin-.3--amine (155 g, 645mmol) in CH3CN (2.50 L), was added (batchwise) tert-butyl 4-(cyanomethyiidene)piperidine--i--carboxylate (286 g. 1.29 mol) followed by dropwise addition of DBU (99.0 g, 650 mmol) at 20°C over 20 minutes. The resulting solution was stirred for 3 days at 20°C, concentrated in vacuo at 40---45°C, and then purified by silica chromatography, eluting with 0---50% ethyl acetate/hexanes, Concentration of the desired fraction in vacuo afforded the title compound.LRMS (ES1) caic’d for C25H31N603 [M+Hf: 463, found 463. ‘H NMR (300 MHz, CDCi3): 67.82 (ci, 1H), 734-750 (in, SF1), 6.84 (ci, 1H), 554 (s, 2H), 4.51 (hr s, 2H), 3.94-3.97 (d, 2H),3.05 (br s, 2H), 2.85-2.90 (m, 2H), 2.79 (s, 2K), 1.92-2.04 (in, 2H), 1.45 (s, 9H).
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