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[ CAS No. 113975-22-7 ] {[proInfo.proName]}

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Chemical Structure| 113975-22-7
Chemical Structure| 113975-22-7
Structure of 113975-22-7 * Storage: {[proInfo.prStorage]}

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Product Details of [ 113975-22-7 ]

CAS No. :113975-22-7 MDL No. :MFCD03095287
Formula : C5H3FIN Boiling Point : No data available
Linear Structure Formula :- InChI Key :WCDCAXVNBOLWNO-UHFFFAOYSA-N
M.W : 222.99 Pubchem ID :7009501
Synonyms :

Calculated chemistry of [ 113975-22-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 8
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 : 36.91
TPSA : 12.89 ?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) : -6.28 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.66
Log Po/w (XLOGP3) : 1.94
Log Po/w (WLOGP) : 2.25
Log Po/w (MLOGP) : 1.85
Log Po/w (SILICOS-IT) : 2.83
Consensus Log Po/w : 2.11

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.0
Solubility : 0.223 mg/ml ; 0.001 mol/l
Class : Soluble
Log S (Ali) : -1.84
Solubility : 3.26 mg/ml ; 0.0146 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -3.26
Solubility : 0.122 mg/ml ; 0.000548 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.2

Safety of [ 113975-22-7 ]

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

Application In Synthesis of [ 113975-22-7 ]

* 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.

  • Downstream synthetic route of [ 113975-22-7 ]

[ 113975-22-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 113975-22-7 ]
  • [ 109-94-4 ]
  • [ 171366-19-1 ]
YieldReaction ConditionsOperation in experiment
708 mg (62%) With n-butyllithium; sodium borohydrid; diisopropylamine; In tetrahydrofuran; ethyl acetate; EXAMPLE 1 2-Fluoro-4-iodo-3-(hydroxymethyl)pyridine To a solution of LDA, freshly prepared from diisopropylamine (0.63 mL, 4.49 mmol) and n-BuLi (4.49 mmol) in THF (10 mL) at -78 C., is cannulated a solution of 2-fluoro-3-iodopyridine (1 g, 4.48 mmol) in 2 mL of THF, and the mixture is stirred for 1 hour at -78 C. under nitrogen. Ethyl formate (1.1 mL, 13.6 mmol) is added to the reaction mixture at -78 C. and stirring is continued for 30 min. The reaction is quenched with saturated sodium bicarbonate solution at -78 C. and allowed to warm to room temperature. Sodium borohydride (0.34 g, 8.99 mmol) is slowly added to the reaction mixture and then stirred for 30 min. The mixture is extracted with ethyl acetate. The combined ethyl acetate extracts are washed with brine, dried (MgSO4) and concentrated in vacuo. The residue is purified by radial plc (silica gel, hexanes, 10% EtOAc/hexanes, 20% EtOAc/hexanes) to afford 708 mg (62 %) of the product as a white solid having a mp of 69-70 C. Elemental Analysis for C6 H5 FINO: theory: C 28.48, H 1.99, N 5.54; found: C 28.55, H 1.94, N 5.48. IR (KBr): cm1 3336, 1584, 1541, 1446, 1401, 1264, 1218, 1003, 870, 833,803,761,577. 1 H NMR (CDCl3): delta7.79-7.82 (d, 1H,J=5 Hz), 7.66-7.68 (d, 1H, J=5 Hz), 4.82-4.86 (d, 2H, J=7 Hz), 1.99-2.04 (t, 1H, J=14 Hz). 13 C NMR (CDCl3): delta 162.29, 159.05, 147.30, 147.09, 132.79, 132.73,126.14, 125.73, 114.21, 62.24.
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