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Chemical Structure| 853685-35-5 Chemical Structure| 853685-35-5

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Chemical Structure| 853685-35-5

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Product Details of [ 853685-35-5 ]

CAS No. :853685-35-5
Formula : C8H7N3O
M.W : 161.16
SMILES Code : O=C(C1=CC2=NC=CC=C2N1)N
MDL No. :MFCD12924483

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Application In Synthesis of [ 853685-35-5 ]

* 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.

  • Downstream synthetic route of [ 853685-35-5 ]

[ 853685-35-5 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 17288-32-3 ]
  • [ 853685-35-5 ]
YieldReaction ConditionsOperation in experiment
~ 100% With ammonia; In water; at 20℃;Product distribution / selectivity; Suspend ester 4a-1 in concentrated NH4OH and stir at rt for several days monitoring by tlc (10percent MeOH/CH2Cl2). When complete, concentrate the reaction to minimum volume, dilute with excess H2O, collect the precipitate by filtration and dry to give amide 6a-1 (R2NH2, R4H) in about quantitative yield.
> 90% With ammonia; lithium chloride; In methanol; at 20℃; for 120h;Product distribution / selectivity; Stir ethyl 4-aza-2-indole carboxylate 4a (4.67 mmol) in 7N NH3/MeOH (20 mL) and add LICl (1.0 equiv, 4.67 mmol). Stir the reaction at rt for 5 days monitoring by tlc (10percent MeOH/CH2Cl2) during which time a precipitate forms. Concentrate the mixture to minimum volume, dilute with H2O and collect the solid by filtration. Wash the filter cake with H2O and dry under vacuum at 60° C. to afford primary amide 6a (>90percent).
44 - ~ 100% With ammonia; In methanol; at 20 - 55℃; under 517.162 - 1810.07 Torr;Product distribution / selectivity; 1H-Pyrrolo[3,2-b]pyridine-2-carboxylic acid amide, 6a-1 (Scheme 1, step e) Add a solution of 7 N NH3 in MeOH (1.5 L, 10.5 mol, 20 equiv.) to a 3-L pressure reactor at rt and then add azaindole ester 4a-1 (100 g, 0.53 mol) as a solid. Slowly heat the slurry to 50° C. to afford a clear solution. One observes the initial pressure of 35 psi to drop to 16 psi over 4 h. Maintain the reaction at 50° C. for 49 h. One observes a final pressure of 10 psi. Monitor the progress of the reaction by HPLC (Agilent series 1100 using the following conditions: Waters Symmetry C8 (5mu) column (3.9*150 mm), flow rate at 1.0 mL/min, gradient elution conditions: time (minutes), water:acetonitrile-methanol ratio (acetonitrile-methanol used as a 1:1 solution) 0 min., 70:30; 10 min., 20:80; 15 min., 70:30; 20 min., 70:30; lambda1=210 nm, lambda2=220 nm, flow rate 1.0 mL/min, RT: ethyl ester 4a-1=5.6 min, methyl ester 5a-1=4.2 min, amide 6a-1=2.2 min). One observes the corresponding methyl ester 5a-1 being formed in the reaction and 5a-1 serves also as an intermediate in the reaction. Cool the reaction to 4° C. and isolate the resulting precipitate by vacuum filtration. Wash the filter cake with methyl tert-butyl ether (2*100 mL) and dry (40° C./0.1 in Hg) for 20 h to give 6a-1 as a gray solid (78.6 g, 93percent). 1H NMR (DMSO-d6) delta 7.17 (dd, 1H, J=4.5, 8.4 Hz), 7.53, 8.11 (2s, 2H, NH2), 7.76 (d, 1H, J=8.1 Hz), 8.37 (d, 1H, J=1.5 Hz), 11.72 (s, 1H, NH).
24% With ammonia; In ethanol; at 90℃; for 12h;Inert atmosphere; To a stirred solution of ethyl lH-pyrrolo[3,2-£]pyridine-2-carboxylate 1 (300 mg, 1.58 mmol) in EtOH (6 mL) in a steel bomb at RT under an inert atmosphere, was added NH3 solution (18 mL). The reaction mixture was sealed and heated at 90 °C for 12 h. The reaction mixture was cooled to RT and concentrated under reduced pressure. The residue was diluted with water (20 mL) and extracted with EtOAC (2 x 30 mL). The combined organic extracts were washed with brine (15 mL), dried (Na2S04), filtered, and concentrated under reduced pressure to afford compound 2 (60 mg, 24percent) as an off-white solid. 1H MR (500 MHz, OMSO-d6): delta 11.77 (br s, 1H), 8.38 (br d, J= 3.3 Hz, 1H), 8.11 (br s, 1H), 7.76 (br d, J= 8.3 Hz, 1H), 7.54 (br s, 1H), 7.25 (s, 1H), 7.18 (dd, J= 8.3, 4.4 Hz, 1H); LCMS Mass: 162.1 (M++l).

  • 2
  • [ 67-56-1 ]
  • [ 17288-32-3 ]
  • [ 394223-19-9 ]
  • [ 853685-35-5 ]
  • [ 17288-35-6 ]
  • 3
  • [ 17288-32-3 ]
  • [ 853685-35-5 ]
  • [ 17288-35-6 ]
 

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