| Identification | Back Directory | [Name]
D-xylo-Pentodialdo-5,2-furanose, 4,5-O-(1-Methylethylidene)-1-C-4-Morpholinyl-,(5S)- | [CAS]
1103738-19-7 | [Synonyms]
SOTA-005
EOS-61383
LX-4211 int
6aS)-6-hydroxy-2
LX-4211 inermediate
LX-4211 intermediate
2-dimethyltetrahydrofuro[2
3]dioxol-5-yl)(morpholino)methanone
(5S)-4,5-O-(1-Methylethylidene)-1-C-4-morpholinyl-D-xylo-pentodialdo-5,2-furanose
D-xylo-Pentodialdo-5,2-furanose, 4,5-O-(1-Methylethylidene)-1-C-4-Morpholinyl-,(5S)-
((3aS,5R,6S,6aS)-6-hydroxy-2,2-diMethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl)(Morpholino)Methanone
((3aS,5S,6R,6aS)-6-hydroxy-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl)(morpholino)methanone
(3aS,5R,6S,6aS)-[6-hydroxy-2,2-dimethyltetrahydrofuro[3,2-d][1,3]dioxol-5-yl]-(morpholino)methanone
[(3aS,5R,6S,6aS)-6-hydroxy-2,2-dimethyl-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxol-5-yl]-morpholin-4-ylmethanone | [Molecular Formula]
C12H19NO6 | [MDL Number]
MFCD25977365 | [MOL File]
1103738-19-7.mol | [Molecular Weight]
273.28 |
| Chemical Properties | Back Directory | [Boiling point ]
479.3±45.0 °C(Predicted) | [density ]
1.318±0.06 g/cm3(Predicted) | [storage temp. ]
Storage temp. 2-8°C | [pka]
12.78±0.60(Predicted) | [Appearance]
Off-white to yellow Solid | [InChI]
InChI=1S/C12H19NO6/c1-12(2)18-9-7(14)8(17-11(9)19-12)10(15)13-3-5-16-6-4-13/h7-9,11,14H,3-6H2,1-2H3/t7-,8-,9+,11+/m1/s1 | [InChIKey]
ZHDDJWFZDNKWIC-REIXXSIJSA-N | [SMILES]
O=C(N1CCOCC1)[C@H]1[C@H]([C@H]2[C@@]([H])(O1)OC(O2)(C)C)O |
| Hazard Information | Back Directory | [Synthesis]
To a solution of (3aS,5R,6S,6aS)-6-hydroxy-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxole-5-carboxylic acid (5.0 g, 24.5 mmol) in THF (100 ML, 20.x.) was added TBTU (11.8 g, 1.5 equiv), N-methylmorpholine (NMM, 4.1 mL, 1.5 equiv) and the mixture was stirred at 20° C. for 30 min. Morpholine (3.2 mL, 1.5 equiv) was added, and the reaction mixture was stirred at 20° C. for an additional 6h. The solid was filtered off by filtration, and the cake was washed with THF (10 mL, 2.x. .x.2). The organic solution was concentrated under a vacuum. The residue was purified by silica gel column chromatography (hexanes: EtOAc, from 1:4 to 4: 1) to afford 4.3 g of the desired morpholine amide (((3AS,5R,6S,6aS)-6-hydroxy-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl)(morpholino)methanone) as a white solid.
| [References]
[1] Patent: US2009/30198, 2009, A1. Location in patent: Page/Page column 8
[2] Patent: US2010/16422, 2010, A1. Location in patent: Page/Page column 4
[3] Patent: EP2332947, 2011, A1. Location in patent: Page/Page column 6-7
[4] Patent: EP2661256, 2018, B1. Location in patent: Paragraph 0091
[5] Patent: CN106892948, 2017, A. Location in patent: Paragraph 0195; 0196; 0197; 0198 |
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