* 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.
Reference：
[1] Yakugaku Zasshi, 1931, vol. 51, p. 542,571; dtsch. Ref. S. 73, 76[2] Chem.Abstr., 1931, p. 5427
6
[ 5332-24-1 ]
[ 98555-51-2 ]
Yield
Reaction Conditions
Operation in experiment
48%
Stage #1: With ruthenium(IV) oxide; sodium hypochlorite In tetrachloromethane for 24 h; Stage #2: With hydrogenchloride; water In tetrachloromethane
Example 12 2-Bromo-7-(4-fluoro-benzyl)-5,9-dihydroxy-pyrrolo[3,4-g]quinoline-6,8-dione 1008 Following the literature procedure of M.-D. Le Bas et al. (Synthesis 2001, 16, p. 2495), 100 ml CCl4 was mixed with 250 ml of an aqueous NaOCl solution. To this mixture was added 40 mg of RuO2, followed by 3 g 3-bromoquinoline dissolved in 50 ml CCl4. Additional 30 ml portions of bleach were added at 2, 4, and 6 h. After 24 h, the aqueous layer was collected and acidified to pH 1 with 3N HCl. The aqueous layer was then extracted with ethyl acetate, dried over Na2SO4 and volatiles removed by evaporation to give the 1.7 g product as a yellow resin, (48percent yield). 1H NMR and MS data matched that reported in the literature. The resulting anhydride, 1 g, was then carried through the previously reported multistep sequence to afford the corresponding cyano-ester. Dieckmann condensation between 80 mg (0.3 mmol) of the ester and 80 mg (3.6 mmol) of the imide utilizing 900 uL LiHMDS in 2 ml dry THF gave the crude product. After the typical work-up, approximately 60 mg (30percent) of unpurified product was obtained as a yellow solid which was further refined by trituration with diethyl ether to provide 2 mg highly pure product 1008. 1H NMR (300 MHz, d6-DMSO) δ 9.20 (d, 1H), 9.05 (d, 1H) and 4.85 (s, 2H) ppm, MS=416.1 (M+H).
25%
With potassium permanganate In methanol; water at 20 - 80℃; for 1.5 h;
To a mixture of 3-bromoquinoline (10 ml, 72.7 mmol) and water (20OmL) was added KMnO4 (69.0 g, 436 mmol) at 6 portion each 15 min at 80°C with stirring. After allowing the reaction to cool to rt, MeOH (20 mL) was added to the solution. The resulting mixture was washed with toluene (100 mL)5 and the aqueous layer was adjusted to pH 1 with cone. HCl. The mixture was extracted twice with EtOAc/THF (10OmL / 50 mL). The combined extracts were washed with brine, dried over Na2SO4, and the solvent was removed in vacuo. Water was added to the residue, the resulting insoluble materials were filtered off. Isobutyl acetate was added to the filtrate, and then water was removed in vacuo. The resulting precipitates were collected by filtration, and dried to give 4.45 g of compound B-2 (yield = 25 percent) as a colorless crystal. EPO <DP n="48"/>1H NMR (DMSO-(IO) δ 12.5O(1H, s), 8.9O(1H, d, J = 2.1 Hz), 8.43(1H, d, J = 2.1 Hz).
Reference：
[1] Journal of Labelled Compounds and Radiopharmaceuticals, 2001, vol. 44, p. S283 - S285
[2] Synthesis, 2001, # 16, p. 2495 - 2499
[3] Patent: US2008/58315, 2008, A1, . Location in patent: Page/Page column 25-26
[4] Patent: WO2007/19098, 2007, A2, . Location in patent: Page/Page column 46-47
7
[ 5332-24-1 ]
[ 110-19-0 ]
[ 98555-51-2 ]
Yield
Reaction Conditions
Operation in experiment
25%
With potassium permanganate In water
Compound B-2: 5-Bromo-pyridine-2,3-dicarboxylic acid To a mixture of 3-bromoquinoline (10 ml, 72.7 mmol) and water (200 mL) was added KMnO4 (69.0 g, 436 mmol) at 6 portion each 15 min at 80° C. with stirring. After allowing the reaction to cool to rt, MeOH (20 mL) was added to the solution. The resulting mixture was washed with toluene (100 mL), and the aqueous layer was adjusted to pH 1 with conc. HCl. The mixture was extracted twice with EtOAc/THF (100 mL/50 mL). The combined extracts were washed with brine, dried over Na2SO4, and the solvent was removed in vacuo. Water was added to the residue, the resulting insoluble materials were filtered off. Isobutyl acetate was added to the filtrate, and then water was removed in vacuo. The resulting precipitates were collected by filtration, and dried to give 4.45 g of compound B-2 (yield=25percent) as a colorless crystal. 1H NMR (DMSO-d6) δ 12.50 (1H, s), 8.90 (1H, d, J=2.1 Hz), 8.43 (1H, d, J=2.1 Hz).
Reference：
[1] Patent: US2015/225399, 2015, A1,
8
[ 69268-39-9 ]
[ 98555-51-2 ]
Reference：
[1] Chemische Berichte, 1886, vol. 19, p. 2884
9
[ 860758-00-5 ]
[ 98555-51-2 ]
Reference：
[1] Justus Liebigs Annalen der Chemie, 1913, vol. 396, p. 27
10
[ 5332-24-1 ]
[ 98555-51-2 ]
[ 5651-01-4 ]
Reference：
[1] Chemische Berichte, 1886, vol. 19, p. 2766
A mixture of <strong>[98555-51-2]5-bromopyridine-2,3-dicarboxylic acid</strong> (41, 10.0 g, 40.6mmol) and acetic anhydride (20 mL, 200 mmol) was stirred at 80 C for 2 h. The reaction mixture wasconcentrated in vacuo, and the residual solid was triturated with hexanes to afford the title compound 42 (8.69 g,94%) as a pale yellow powder
79%
With acetic anhydride; at 80℃; for 1.16667h;Reflux;
A suspension of <strong>[98555-51-2]5-bromo-pyridine-2,3-dicarboxylic acid</strong> (700 mg, 2.85 mmol) in acetic anhydride (0.88 ml, 9.39 mmol, 3.3 equiv.) was heated at 80 C. for 10 min and then refluxed for 1 h. Acetic anhydride was evaporated off in vacuo. The resulting solid was triturated with hexane to afford 3-bromo-furo[3,4-b]pyridine-5,7-dione (510 mg, 79%) as off white solid.
79%
With acetic anhydride; for 1.16667h;Reflux;
A suspension of <strong>[98555-51-2]5-bromo-pyridine-2,3-dicarboxylic acid</strong> (700 mg, 2.85 mmol) in acetic anhydride (0.88 ml, 9.39 mmol, 3.3 equiv.) was heated at 80C for lOmin and then refluxed for lh. Acetic anhydride was evaporated off in vacuo. The resulting solid was triturated with hexane to afford 3-bromo-furo[3,4-b]pyridine-5,7-dione (510 mg, 79%) as off white solid
With acetic anhydride;Heating / reflux;
Example 12 2-Bromo-7-(4-fluoro-benzyl)-5,9-dihydroxy-pyrrolo[3,4-g]quinoline-6,8-dione; 1008 Following the literature procedure of M.-D. Le Bas et al. (Synthesis 2001, 16, p. 2495), 100 ml CCl4 was mixed with 250 ml of an aqueous NaOCl solution. To this mixture was added 40 mg of RuO2, followed by 3 g 3-bromoquinoline dissolved in 50 ml CCl4. Additional 30 ml portions of bleach were added at 2, 4, and 6 h. After 24 h, the aqueous layer was collected and acidified to pH 1 with 3N HCl. The aqueous layer was then extracted with ethyl acetate, dried over Na2SO4 and volatiles removed by evaporation to give the 1.7 g product as a yellow resin, (48% yield). 1H NMR and MS data matched that reported in the literature. The resulting anhydride, 1 g, was then carried through the previously reported multistep sequence to afford the corresponding cyano-ester. Dieckmann condensation between 80 mg (0.3 mmol) of the ester and 80 mg (3.6 mmol) of the imide utilizing 900 uL LiHMDS in 2 ml dry THF gave the crude product. After the typical work-up, approximately 60 mg (30%) of unpurified product was obtained as a yellow solid which was further refined by trituration with diethyl ether to provide 2 mg highly pure product 1008. 1H NMR (300 MHz, d6-DMSO) delta 9.20 (d, 1H), 9.05 (d, 1H) and 4.85 (s, 2H) ppm, MS=416.1 (M+H).
Example 12 2-Bromo-7-(4-fluoro-benzyl)-5,9-dihydroxy-pyrrolo[3,4-g]quinoline-6,8-dione 1008 Following the literature procedure of M.-D. Le Bas et al. (Synthesis 2001, 16, p. 2495), 100 ml CCl4 was mixed with 250 ml of an aqueous NaOCl solution. To this mixture was added 40 mg of RuO2, followed by 3 g 3-bromoquinoline dissolved in 50 ml CCl4. Additional 30 ml portions of bleach were added at 2, 4, and 6 h. After 24 h, the aqueous layer was collected and acidified to pH 1 with 3N HCl. The aqueous layer was then extracted with ethyl acetate, dried over Na2SO4 and volatiles removed by evaporation to give the 1.7 g product as a yellow resin, (48% yield). 1H NMR and MS data matched that reported in the literature. The resulting anhydride, 1 g, was then carried through the previously reported multistep sequence to afford the corresponding cyano-ester. Dieckmann condensation between 80 mg (0.3 mmol) of the ester and 80 mg (3.6 mmol) of the imide utilizing 900 uL LiHMDS in 2 ml dry THF gave the crude product. After the typical work-up, approximately 60 mg (30%) of unpurified product was obtained as a yellow solid which was further refined by trituration with diethyl ether to provide 2 mg highly pure product 1008. 1H NMR (300 MHz, d6-DMSO) delta 9.20 (d, 1H), 9.05 (d, 1H) and 4.85 (s, 2H) ppm, MS=416.1 (M+H).
25%
With potassium permanganate; In methanol; water; at 20 - 80℃; for 1.5h;
To a mixture of 3-bromoquinoline (10 ml, 72.7 mmol) and water (20OmL) was added KMnO4 (69.0 g, 436 mmol) at 6 portion each 15 min at 80C with stirring. After allowing the reaction to cool to rt, MeOH (20 mL) was added to the solution. The resulting mixture was washed with toluene (100 mL)5 and the aqueous layer was adjusted to pH 1 with cone. HCl. The mixture was extracted twice with EtOAc/THF (10OmL / 50 mL). The combined extracts were washed with brine, dried over Na2SO4, and the solvent was removed in vacuo. Water was added to the residue, the resulting insoluble materials were filtered off. Isobutyl acetate was added to the filtrate, and then water was removed in vacuo. The resulting precipitates were collected by filtration, and dried to give 4.45 g of compound B-2 (yield = 25 %) as a colorless crystal. EPO <DP n="48"/>1H NMR (DMSO-(IO) delta 12.5O(1H, s), 8.9O(1H, d, J = 2.1 Hz), 8.43(1H, d, J = 2.1 Hz).
A mixture of compound B-2 (179 g, 728 mmol) and acetic anhydride (1250 niL) was heated at 120C for 1.5 h. After allowing the reaction to cool, acetic anhydride was removed in vacuo. After 2-propanol was added to the residue, the resulting mixture was heated at reflux for 13 h. After allowing the reaction to cool, the solvent was removed in vacuo. The crude product was purified by crystallization with acetone / ('Pr)2O to give 77.8 g of compound B-4 (yield = 37.0 %) as a brown crystal. 1H NMR (CDCl3) delta 8.88(1H, d, J = 2.1 Hz), 8.44(1H, d, J = 2.1 Hz), 7.7O(1H, bs), 5.41-5.28(1H, m), 1.40(6H, d, J = 6.3 Hz).
Compound B-2: 5-Bromo-pyridine-2,3-dicarboxylic acid To a mixture of 3-bromoquinoline (10 ml, 72.7 mmol) and water (200 mL) was added KMnO4 (69.0 g, 436 mmol) at 6 portion each 15 min at 80 C. with stirring. After allowing the reaction to cool to rt, MeOH (20 mL) was added to the solution. The resulting mixture was washed with toluene (100 mL), and the aqueous layer was adjusted to pH 1 with conc. HCl. The mixture was extracted twice with EtOAc/THF (100 mL/50 mL). The combined extracts were washed with brine, dried over Na2SO4, and the solvent was removed in vacuo. Water was added to the residue, the resulting insoluble materials were filtered off. Isobutyl acetate was added to the filtrate, and then water was removed in vacuo. The resulting precipitates were collected by filtration, and dried to give 4.45 g of compound B-2 (yield=25%) as a colorless crystal. 1H NMR (DMSO-d6) delta 12.50 (1H, s), 8.90 (1H, d, J=2.1 Hz), 8.43 (1H, d, J=2.1 Hz).
In ethanol; water; N,N-dimethyl-formamide; at 140℃; for 72h;
(1) A 0.25 mmol (0.0595 g) of NiCl 2 ·6H 2 O was weighed and dissolved in 5 mL of distilled water and 5 mL of absolute ethanol to prepare a nickel chloride solution.(2) Weigh 0.25 mmol (0.0615 g) of <strong>[98555-51-2]5-bromopyridine-2,3-dicarboxylic acid</strong> and 2 mL of DMF, add to a 25 mL beaker, stir until dissolved, and obtain 5-bromopyridine-2,3-di Carboxylic acid solution.(3) The nickel chloride solution obtained in the step (1) is added dropwise to the <strong>[98555-51-2]5-bromopyridine-2,3-dicarboxylic acid</strong> solution prepared in the step (2), and ultrasonically shaken for 20 minutes.Adjust the pH to 6 with ammonia to clarify the solution.The mixture was further shaken for 10 min to prepare a mixed solution.(4) The mixed solution prepared in the step (3) is transferred to a 25 mL reaction vessel with a Teflon bottle and placed in an oven.Heat to 140 C for 72 h, then cool to 90 C at 10 C / h, and then keep warm for 10 h, turn off the oven to make it naturalAfter cooling to room temperature, the reaction vessel was taken out, green needle-like crystals were formed, and washed alternately with acetone and absolute ethanol for 3 times.Each time acetone and absolute ethanol are used in an amount of 5 mL, then placed in a vacuum oven at 50 C and dried for 12 h to obtain a chemical formula of[C7H6BrNNiO6]n nickel complex, which is a nickel complex of 5-bromopyridine-2,3-dicarboxylate. The yield was 73%.
To a solution of 5-bromopyridine-2,3-dicarboxylic acid (5 g, 20.3 mmol) in MeOH (50 mL) was added concentrated H2S04(2 mL). Then the mixture was heated at reflux for 20 h, and TLC showed the reaction was complete. After cooling to r.t., the reaction was quenched with saturated aqueous NaHC03and concentration in vacuo. The residue was diluted with water (50 mL), and then extracted with DCM (50 mL x 3). The combined organic layers were dried over anhydrous Na2S04, filtered, and concentrated in vacuo to give the title compound as a white solid (4.3 g).LC-MS (ESI) found: 275 [M+H]+.
ammonium 6-((((3R,4S,5S,6R)-5-methoxy-4-((2R,3R)-2-methyl-3-(3-methylbut-2-en-1-yl)oxiran-2-yl)-1-oxaspiro[2.5]octan-6-yl)oxy)carbonyl)-6,7-dihydro-5H-pyrrolo[3,4-b]pyridine-3-carboxylate[ No CAS ]
sodium 6-((((3R,4S,5S,6R)-5-methoxy-4-((2R,3R)-2-methyl-3-(3-methylbut-2-en-1-yl)oxiran-2-yl)-1-oxaspiro[2.5]octan-6-yl)oxy)carbonyl)-6,7-dihydro-5H-pyrrolo[3,4-b]pyridine-3-carboxylate[ No CAS ]
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