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CAS No. : | 2924-15-4 | MDL No. : | MFCD00012927 |
Formula : | C6H8ClFN2 | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | VFZYLSYYMHFPSY-UHFFFAOYSA-N |
M.W : | 162.59 | Pubchem ID : | 2723910 |
Synonyms : |
|
Signal Word: | Warning | Class: | N/A |
Precautionary Statements: | P261-P280-P305+P351+P338 | UN#: | N/A |
Hazard Statements: | H302+H312+H332-H315-H319-H335 | Packing Group: | N/A |
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 |
---|---|---|
0.37 g | In ethanol; water; for 2h;Reflux; | To a solution of 2-fluorophenylhydrazinehydrochloride (0.81 g, 5.00 mM) in 30 ml of EtOH/H2O (v/v 5 5/1) <strong>[29882-07-3]4-chloro-1,1-dimethoxybutane</strong> (0.84 g, 5.50 mM) was added and heatedto reflux for 2 hours. Then the solvent was removed under vacuum,and the residue was chromatographed through silica gel eluding withCH2Cl2/MeOH (30:1) to give the 7-fluorotryptamine (0.37 g) as anoil. Subsequently, aq. HCHO (1.56 ml) was added to the solution of7-fluorotryptamine (0.37 g, 2.08mM) in CH3COOH (15ml) in a dropwisemanner. The mixture was stirred at room temperature for 12 hours atthe atmosphere of N2; then the solvent was removed under vacuum, andthe residue was chromatographed through silica gel eluding withCH2Cl2/MeOH (40:1) to afford the 8-fluoro-1,3,4,9-tetrahydro-b-carboline(0.36 g) as a white powder. Finally, to a solution of phenylacetic acid(283 mg, 2.08 mM) in anhydrous N,N-Dimethylformamide (3 ml) wereadded 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride(518 mg, 2.70 mM) and N-Hydroxybenzotriazole (309 mg, 2.29 mM)at 0°C, and then 8-fluoro-1,3,4,9-tetrahydro-b-carboline (0.36 g, 1.89mM)was added to the mixture after stirring for 15 minutes. The mixturewas stirred for another 3 hours, diluted with H2O, and extracted withEtOAc. The combined organic phase was dried over anhydrousNa2SO4, concentrated, and chromatographed over silica gel to give 0.54 g of LG308. |
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