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[ CAS No. 917572-28-2 ] {[proInfo.proName]}

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Chemical Structure| 917572-28-2
Chemical Structure| 917572-28-2
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Product Details of [ 917572-28-2 ]

CAS No. :917572-28-2 MDL No. :MFCD10687133
Formula : C12H16ClNO Boiling Point : -
Linear Structure Formula :- InChI Key :MSRCVCNYPADFER-GFCCVEGCSA-N
M.W : 225.71 Pubchem ID :27281585
Synonyms :

Calculated chemistry of [ 917572-28-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 15
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.5
Num. rotatable bonds : 3
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 66.02
TPSA : 12.47 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : Yes
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.23 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.33
Log Po/w (XLOGP3) : 2.04
Log Po/w (WLOGP) : 1.59
Log Po/w (MLOGP) : 2.02
Log Po/w (SILICOS-IT) : 2.84
Consensus Log Po/w : 2.16

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.62
Solubility : 0.538 mg/ml ; 0.00238 mol/l
Class : Soluble
Log S (Ali) : -1.93
Solubility : 2.65 mg/ml ; 0.0117 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -3.79
Solubility : 0.037 mg/ml ; 0.000164 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.36

Safety of [ 917572-28-2 ]

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 [ 917572-28-2 ]

* 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 [ 917572-28-2 ]

[ 917572-28-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 101376-26-5 ]
  • [ 917572-28-2 ]
YieldReaction ConditionsOperation in experiment
94% With thionyl chloride;N,N-dimethyl-formamide; In dichloromethane; for 2.5h;Heating / reflux; (a) (3S)-4-Benzyl-3-(chloromethyl)morpholine; To a solution of [(3i?)-4-benzykciotaorpholin-3-yl]methanol (see J. Med. Chem.; 29; 1986; 0 1288-1290; 1.83 g, 8.8 mmol) in dry methylene chloride (15 mL) was added thionyl chloride (3.15 g, 26.5 mmol) and DMF (2 drops). The mixture was heated to reflux for 2 h 30 min and then the solvent was removed by evaporation. The residue was treated with aqueous NaHCO3 and the solution was extracted with ethyl acetate. The organic solution was separated and the solvent was removed by evaporation. There was obtained 1.88 g s (94%) of (31S)-4-benzyl-3-(chloromethyl)morpholine as an oil. 1H NMR (500 MHz, CDCl3): 2.3-2.4 (m, IH), 2.7 (m, IH), 2.8 (m, IH), 3.5 (d, IH), 3.6-3.9 (m, 5H), 4.0 (d, IH), 7.3 (m, IH), 7.4 (m, 4H); LCMS: m/z 226 (M+l)+.
94% With thionyl chloride; N,N-dimethyl-formamide; In dichloromethane; for 2.5h;Heating / reflux; (a) (3S)-4-Benzyl-3-(chloromethyl)morpholineTo a solution of [(3i?)-4-benzylmorpholin-3-yl]methanol (see J. Med. Chem.; 29; 1986; 1288-1290; 1.83 g, 8.8 mmol) in dry methylene chloride (15 mL) was added thionyl chloride (3.15 g, 26.5 mmol) and DMF (2 drops). The mixture was heated to refluxed for 2 h 30 min and then the solvent was removed by evaporation. The residue was treated with aqueous NaHCO3 and the solution was extracted with ethyl acetate. The organic solution was separated and the solvent was removed by evaporation. There was obtained 1.88 g (94%) of (3S)-4-berLzyl-3-(chloromethyl)morpholine as an oil. 1H NMR (500 MHz, CDCl3): 2.3-2.4 (m, IH), 2.7 (m, IH), 2.8 (m, IH), 3.5 (d, IH), 3.6-3.9 (m, 5H), 4.0 (d, IH), 7.3 (m, IH), 7.4 (m, 4H); LCMS: m/z 226 (M+l)+.
With thionyl chloride; In dichloromethane; for 15h; Intermediate 64(S)-4-Benzyl-3-(chloromethyl)morpholine[0349][Chemical Formula 95]To a solution of intermediate 65 (9.60 g, 46.3 mmol) in dichloromethane (230 mL) was added thionyl chloride (60.0 mL, 69.5 mmol). After stirring for 15 hours, to the mixture was added aqueous sodium hydroxide solution. The aqueous layer was neutralized with 2N hydrochloric acid, and then extracted with dichloromethane. The organic layer was washed with water and brine, and then dried over sodium sulfate, and concentrated under reduced pressure to give the title compound (10.4 g, 46.3 mmol, quant.).MS (ESI+) 226 (M++l, 100%)
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