1H-Pyrrolo[2,3-c]pyridine-5-carboxylicacid(9CI)

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1H-Pyrrolo[2,3-c]pyridine-5-carboxylicacid(9CI) Basic information
Product Name:1H-Pyrrolo[2,3-c]pyridine-5-carboxylicacid(9CI)
Synonyms:1H-Pyrrolo[2,3-c]pyridine-5-carboxylicacid(9CI);1H-Pyrrolo[2,3-c]pyridine-5-carboxylic acid;6-Azaindole-5-carboxylic acid
CAS:130473-27-7
MF:C8H6N2O2
MW:162.15
EINECS:
Product Categories:GLYCINESCAFFOLD
Mol File:130473-27-7.mol
1H-Pyrrolo[2,3-c]pyridine-5-carboxylicacid(9CI) Structure
1H-Pyrrolo[2,3-c]pyridine-5-carboxylicacid(9CI) Chemical Properties
Boiling point 471.1±25.0 °C(Predicted)
density 1.506±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
pka1.40±0.30(Predicted)
AppearanceYellow to brown Solid
Safety Information
MSDS Information
1H-Pyrrolo[2,3-c]pyridine-5-carboxylicacid(9CI) Usage And Synthesis
Synthesis
1H-Pyrrolo[2,3-c]pyridine-5-carboxaldehyde (9CI)

130473-26-6

1H-Pyrrolo[2,3-c]pyridine-5-carboxylicacid(9CI)

130473-27-7

1H-pyrrolo[2,3-c]pyridine-5-carboxaldehyde (500 mg, 3.42 mmol) was used as starting material, which was dissolved in 1.5 mL of formic acid. The reaction solution was cooled in an ice bath, and 30% aqueous hydrogen peroxide solution (722 μL, 6.8 mmol) was added slowly and dropwise, keeping the reaction system stirred in an ice bath for 1 h. The reaction system was then left to stand at 5 °C overnight. Upon completion of the reaction, the reaction solution was diluted with deionized water, and the resulting solid was collected, washed with deionized water and dried to give 522 mg of an off-white solid. The formate was dissolved in 7 mL of deionized water, 3 mL of 2N sodium hydroxide solution was added, and the pH was adjusted with 5% aqueous hydrochloric acid to 3. The precipitate precipitated was collected and dried to give 1H-pyrrolo[2,3-c]pyridine-5-carboxylic acid (67% yield). High resolution mass spectrometry (FAB) analysis resulted in a theoretically calculated value of 163.0508 for C8H6N2O2 + H and a measured value of 163.0507 (M + H). In Example 23(i), the target product can be obtained by coupling exo-[2.2.1]-3-amine or endo-[2.2.1]-3-amine with 1H-pyrrolo[2,3-c]pyridine-5-carboxylic acid.

References[1] Tetrahedron, 1990, vol. 46, # 9, p. 3245 - 3266
[2] Synthesis, 1993, # 3, p. 295 - 297
[3] Patent: US2003/153595, 2003, A1
[4] Patent: US2003/45540, 2003, A1
[5] Patent: WO2004/39815, 2004, A2. Location in patent: Page 58
Tag:1H-Pyrrolo[2,3-c]pyridine-5-carboxylicacid(9CI)(130473-27-7) Related Product Information
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