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[ CAS No. 203661-69-2 ] {[proInfo.proName]}

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Chemical Structure| 203661-69-2
Chemical Structure| 203661-69-2
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Product Details of [ 203661-69-2 ]

CAS No. :203661-69-2 MDL No. :MFCD12198552
Formula : C13H21NO3 Boiling Point : -
Linear Structure Formula :- InChI Key :SIMIIXFMGJYGLR-UHFFFAOYSA-N
M.W : 239.31 Pubchem ID :11195798
Synonyms :
Chemical Name :tert-Butyl 2-oxo-7-azaspiro[3.5]nonane-7-carboxylate

Calculated chemistry of [ 203661-69-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 17
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.85
Num. rotatable bonds : 3
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 68.84
TPSA : 46.61 ?2

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) : -6.93 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.62
Log Po/w (XLOGP3) : 1.17
Log Po/w (WLOGP) : 1.99
Log Po/w (MLOGP) : 1.6
Log Po/w (SILICOS-IT) : 1.94
Consensus Log Po/w : 1.86

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.86
Solubility : 3.28 mg/ml ; 0.0137 mol/l
Class : Very soluble
Log S (Ali) : -1.74
Solubility : 4.31 mg/ml ; 0.018 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.22
Solubility : 1.45 mg/ml ; 0.00605 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.69

Safety of [ 203661-69-2 ]

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

Application In Synthesis of [ 203661-69-2 ]

* 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 [ 203661-69-2 ]

[ 203661-69-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 38573-88-5 ]
  • [ 203661-69-2 ]
  • [ 1225276-78-7 ]
YieldReaction ConditionsOperation in experiment
Synthesis of 2-(2,3-difluorophenyl)-7-azaspiro[3.5]nonane hydrochloride; To a solution of tert-butyl 2-oxo-7-azaspiro[3.5]nonane-7-carboxylate (2.48 g, 10.36 mmol) in THF (50 mL) at 0° C. was added 2,3-difluorophenylmagnesium bromide (prepared from stirring <strong>[38573-88-5]1-<strong>[38573-88-5]bromo-2,3-difluorobenzene</strong></strong> (4.00 g, 20.73 mmol) and isopropyl magnesium chloride (15.7 mL, 20.4 mmol) in THF (10 mL) at r.t. for 14 hrs). After 1 h, the reaction was quenched with saturated ammonium chloride and extracted with ethyl acetate. The organic layers were dried over sodium sulfate, filtered, and concentrated to give the crude alcohol as a pale yellow oil. A solution of the crude alcohol and triethylsilane (7.0 mL, 44.0 mmol) in methylene chloride (50 mL) was treated with borontrifluoride diethyl etherate (2.56 mL, 20.7 mmol) and trifluoroacetic acid (3.9 mL, 52.0 mmol) at 0° C. After 1 h at 0° C., the reaction was quenched with saturated sodium bicarbonate and extracted with dichloromethane. The organics were washed with brine, dried over magnesium sulfate, filtered, and concentrated. The oil was diluted with ether and treated with 4N HCl/dioxane (4 mL). The precipitate was filtered and dried to give the title compound as a white solid (1.5 g, 61percent).
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