3(S)-HYDROXYMETHYLMORPHOLINE
3(S)-HYDROXYMETHYLMORPHOLINE Basic information
- Product Name:
- 3(S)-HYDROXYMETHYLMORPHOLINE
- Synonyms:
-
- (3S)-3-Morpholinemethanol
- (3S)-3-Morpholinemethanol,99%e.e.
- (S)-3-Hydroxymethylmorpholine
- (S)-morpholin-3-ylmethanol
- 3-Morpholinemethanol, (3S)-
- (3S)-morpholin-3-ylmethanol
- 3(S)-HYDROXYMETHYLMORPHOLINE
- (3S)-3-(Hydroxymethyl)morpholine
- CAS:
- 211053-50-8
- MF:
- C5H11NO2
- MW:
- 117.15
- Product Categories:
-
- pharmacetical
- Mol File:
- 211053-50-8.mol
3(S)-HYDROXYMETHYLMORPHOLINE Chemical Properties
- Melting point:
- 112 °C
- Boiling point:
- 218.3±20.0 °C(Predicted)
- Density
- 1.045±0.06 g/cm3(Predicted)
- storage temp.
- 2-8°C
- pka
- 14.85±0.10(Predicted)
- Appearance
- Off-white to brown Solid
3(S)-HYDROXYMETHYLMORPHOLINE Usage And Synthesis
Uses
(S)-3-Hydroxymethylmorpholine is a chemical reagent used in the synthesis of Aurora kinase inhibitors, used for their anti-tumor activity. Also used in the preparation of human epidermal growth factor receptor 1 & 2 kinase inhbitors in the treatment of solid tumors.
Synthesis
101376-25-4
211053-50-8
To a solution of (S)-(4-benzylmorpholin-3-yl)methanol (10.0 g, 48.3 mmol) in methanol (300 mL) was added 10 wt% of carbon-loaded palladium catalyst (2.0 g), and the reaction mixture was transferred to a Parr reactor. The reaction was carried out for 18 hours at room temperature under hydrogen pressure of 50 psi. Upon completion of the reaction, the mixture was filtered through a Celite pad to remove the catalyst. The filtrate was concentrated under reduced pressure to afford (S)-3-hydroxymethylmorpholine (5.2 g, 92% yield) as a colorless oil.1H NMR (CDCl3) δ: 3.81-3.76 (2H, m), 3.58-3.43 (3H, m), 3.35-3.28 (1H, m), 2.99-2.91 (5H, br.m). Mass spectrum (ES+) m/z: 118.0 ([M + H]+).
References
[1] Patent: WO2008/47109, 2008, A1. Location in patent: Page/Page column 41
[2] Patent: WO2009/1089, 2008, A1. Location in patent: Page/Page column 29-30
[3] Patent: WO2009/71895, 2009, A1. Location in patent: Page/Page column 110
[4] Patent: US2011/3785, 2011, A1. Location in patent: Page/Page column 11
[5] Patent: WO2006/114606, 2006, A1. Location in patent: Page/Page column 78
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3(S)-HYDROXYMETHYLMORPHOLINE(211053-50-8)Related Product Information
- (S)-N-BOC-2-HYDROXYMETHYLMORPHOLINE,(S)-2-Hydroxymethylmorpholine-4-carboxylic acid tert-butyl ester
- 2-HYDROXYMETHYLMORPHOLINE,2-HYDROXYMETHYLMORPHOLINE 95%
- (R )-2-Hydroxymethylmorpholine,(R)-2-Hydroxymethylmorpholine HCl
- (R)-3-MORPHOLINECARBOXYLIC ACID HCL
- 4-Boc-3(R)-morpholinecarboxylic acid
- (S)-3-Hydroxymethylmorpholine-4-carboxylic acid tert-butyl ester
- (R)-4-Boc-3-hydroxymethylmorpholine
- (R)-N-BOC-2-HYDROXYMETHYLMORPHOLINE,(R)-2-Hydroxymethylmorpholine-4-carboxylic acid tert-butyl ester
- 4-N-BOC-2-HYDROXYMETHYLMORPHOLINE
- (S)-4-BENZYL-3-HYDROXYMETHYLMORPHOLINE
- 4-FMOC-3(R)-MORPHOLINECARBOXYLIC ACID
- 3(S)-HYDROXYMETHYLMORPHOLINE
- (R)-3-Hydroxymethylmorpholine,3(R)-HYDROXYMETHYLMORPHOLINE HCL,,3(R)-HYDROXYMETHYLMORPHOLINE
- 4-CBZ-2-HYDROXYMETHYLMORPHOLINE
- (R)-4-BENZYL-3-HYDROXYMETHYLMORPHOLINE
- N-BOC-3-hydroxymethylmorpholine
- (S)-N-BENZYL-2-HYDROXYMETHYLMORPHOLINE
- 4-BENZYL-3-HYDROXYMETHYLMORPHOLINE