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CAS No. : | 18797-86-9 | MDL No. : | MFCD00050910 |
Formula : | C22H26N2O3 | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | - |
M.W : | 366.45 | Pubchem ID : | - |
Synonyms : |
|
Signal Word: | Warning | Class: | |
Precautionary Statements: | P264-P270-P280-P301+P312+P330-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313-P501 | UN#: | |
Hazard Statements: | H302-H315-H319 | Packing Group: | |
GHS Pictogram: |
* 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.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With hydrogenchloride; KH2PO4 buffer In acetonitrile at 65℃; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With d(4)-methanol at 21 - 22℃; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
96% | With Selectfluor In acetonitrile |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
99% | With triethylamine | |
99% | In dichloromethane at 20℃; for 24h; Inert atmosphere; | |
81% | In dichloromethane at 20℃; for 17h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
1: 20% 2: 20% 3: 20% 4: 10% | With hydrogen fluoride; dihydrogen peroxide; antimony pentafluoride at -35℃; for 0.05h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
In dichloromethane at 20℃; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
In [D3]acetonitrile |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
In dichloromethane at 20℃; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
58% | Stage #1: (R)-(6-methoxyquinolin-4-yl)((2S,4S,5R)-5-vinylquinuclidin-2-yl)methyl acetate With boron tribromide In dichloromethane at -78℃; Inert atmosphere; Stage #2: With ammonia; water In dichloromethane at 0 - 20℃; Inert atmosphere; | 2.4 (R)-(6-Hydroxyquinolin-4-yl)((2S,4S,5R)-5-vinylquinuclidin-2-yl)methyl acetate Q-526 Q-5 was prepared from O-acetylquinine27 according to the literature procedure and similar to QD-2, white solid, 58% yield. 1H NMR (400 MHz, CDCl3): δ 8.67 (d, J = 4.5 Hz, 1H), 7.97 (d, J = 9.2 Hz, 1H), 7.55 (d, J = 2.6 Hz, 1H), 7.34-7.25 (m, 2H), 6.57 (d, J = 5.7 Hz, 1H), 6.05-5.96 (m, 2H), 5.13-5.08 (m, 2H), 3.34-3.26 (m, 1H), 3.05-2.91 (m, 2H), 2.83-2.69 (m, 2H), 2.32-2.26 (m, 1H), 2.12 (s, 3H), 1.98-1.85 (m, 1H), 1.82 (s, 1H), 1.57-1.45 (m, 2H), 1.40-1.32 (m, 1H). |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
80% | With 4-tolyl iodide; Olah′s reagent; Selectfluor In 1,2-dichloro-ethane at 20℃; for 14h; Sealed tube; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
88% | With pyridine at 0 - 20℃; for 21h; Inert atmosphere; |
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