ChemicalBook--->CAS DataBase List--->350595-57-2

350595-57-2

350595-57-2 Structure

350595-57-2 Structure
IdentificationBack Directory
[Name]

3S-3-METHYLMORPHOLINE
[CAS]

350595-57-2
[Synonyms]

3S-3-METHYLMORPHOLINE
(S)-3-Methylmorpholine
(S)-3-MethylMorpholine HCl
Morpholine, 3-Methyl-, (3S)-
3S-3-Methylmorpholine(WX604204)
[Molecular Formula]

C5H11NO
[MDL Number]

MFCD03840369
[MOL File]

350595-57-2.mol
[Molecular Weight]

101.15
Chemical PropertiesBack Directory
[Boiling point ]

137.1±15.0 °C(Predicted)
[density ]

0.891±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,2-8°C
[form ]

liquid
[pka]

9.03±0.40(Predicted)
[color ]

colourless
[Optical Rotation]

Consistent with structure
[InChI]

InChI=1S/C5H11NO/c1-5-4-7-3-2-6-5/h5-6H,2-4H2,1H3/t5-/m0/s1
[InChIKey]

SFWWGMKXCYLZEG-YFKPBYRVSA-N
[SMILES]

N1CCOC[C@@H]1C
Hazard InformationBack Directory
[Uses]

It is useful in preparation of morpholinopyrimidine derivatives as mTOR kinase inhibitors for the treatment of diseases mediated by mTOR kinase and/or one or more PI3K enzymes
[Synthesis]

(5S)-5-methylmorpholin-3-one

119844-66-5

3S-3-METHYLMORPHOLINE

350595-57-2

Step-4: Synthesis of (S)-3-methylmorpholine (117): lithium aluminum hydride (87 g, 3.0 eq.) was suspended in anhydrous tetrahydrofuran (1500 mL) in a three necked round bottomed flask at 0°C under nitrogen protection. (S)-5-methylmorpholin-3-one (88 g) was dissolved in anhydrous tetrahydrofuran (500 mL) and slowly added dropwise to the reaction system at the same temperature. The reaction mixture was gradually warmed to room temperature and stirred continuously overnight. Upon completion of the reaction, it was quenched sequentially with water (100 mL), 2N sodium hydroxide solution (200 mL), and water (300 mL) (using Fisher post-treatment method) and stirred for 30 minutes. Subsequently, a 2% methanol/dichloromethane mixture (1000 mL) was added and stirring was continued for 1.0 hour. The crude product was filtered through a diatomaceous earth pad, and the filtrate was dried over anhydrous sodium sulfate and finally concentrated on a rotary evaporator at a low water bath temperature of 20-25 °C to afford the target product (S)-3-methylmorpholine (55 g, 71% yield).

[References]

[1] Patent: WO2014/16849, 2014, A2. Location in patent: Page/Page column 126; 127; 128
[2] Synthesis (Germany), 2014, vol. 46,
[3] Patent: US2008/255114, 2008, A1. Location in patent: Page/Page column 17
[4] Patent: EP1785418, 2007, A1. Location in patent: Page/Page column 148
[5] Patent: CN106749081, 2017, A. Location in patent: Paragraph 0016; 0017; 0018; 0019; 0020; 0021
Safety DataBack Directory
[Symbol(GHS) ]

Flame (GHS02)Exclamation Mark (GHS07)
GHS02,GHS07
[Signal word ]

Danger
[Hazard statements ]

H225-H319
[Precautionary statements ]

P210-P233-P240-P241-P242-P243-P264-P280-P303+P361+P353-P305+P351+P338-P337+P313-P370+P378-P403+P235-P501
[Hazard Codes ]

Xn
[Risk Statements ]

22
[RIDADR ]

2735
[HazardClass ]

8
[PackingGroup ]

[HS Code ]

2934999090
Spectrum DetailBack Directory
[Spectrum Detail]

3S-3-METHYLMORPHOLINE(350595-57-2)1HNMR
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