Basic information Safety Supplier Related

6-AMINO-1H-INDAZOLE-7-CARBOXYLIC ACID

Basic information Safety Supplier Related

6-AMINO-1H-INDAZOLE-7-CARBOXYLIC ACID Basic information

Product Name:
6-AMINO-1H-INDAZOLE-7-CARBOXYLIC ACID
Synonyms:
  • 6-AMINO-1H-INDAZOLE-7-CARBOXYLIC ACID
  • 6-Amino-7-carboxy-1H-indazole
  • 7-Carboxy-1H-indazole-6-amine
  • 1H-Indazole-7-carboxylic acid, 6-aMino-
  • TIMTEC-BB SBB002550
CAS:
73907-95-6
MF:
C8H7N3O2
MW:
177.16
Product Categories:
  • Indazoles
Mol File:
Mol File
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6-AMINO-1H-INDAZOLE-7-CARBOXYLIC ACID Chemical Properties

Melting point:
177 °C (decomp)
Boiling point:
501.6±35.0 °C(Predicted)
Density 
1.611
storage temp. 
Sealed in dry,Room Temperature
form 
Solid
pka
16.17±0.40(Predicted)
Appearance
Yellow to brown Solid
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
22
HS Code 
2933998090
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6-AMINO-1H-INDAZOLE-7-CARBOXYLIC ACID Usage And Synthesis

Synthesis

73907-94-5

73907-95-6

Pyrrolo[2,3-g]indazole-7,8(1H,6H)-dione (Formula 7, the product of Example II, 9.4 g, 50 mmol) was used as a raw material, which was dissolved in 10% aqueous sodium hydroxide solution (100 mL). Subsequently, 10% aqueous hydrogen peroxide solution (17 mL, 50 mmol) was slowly added at 100 °C. The reaction mixture was kept at 100°C for 10 minutes until the release of carbon dioxide gas stopped. Next, the pH of the reaction solution was adjusted with concentrated hydrochloric acid to 4.0-5.5. The resulting 6-amino-1H-indazole-7-carboxylic acid (formula 8) was collected by filtration and washed with cold water, and finally dried under vacuum in the presence of CaCl2 to give 7.71 g of the product in brown powder form in 87% yield with a melting point of 205 °C (decomposition started at 177 °C). The infrared spectrum (KBr) of the product showed characteristic absorption peaks: 1580, 1630, 1660 cm-1 (corresponding to aromatic ring and carbonyl carboxylic acid, respectively). The NMR hydrogen spectrum (100 MHz, DMSO-d6) data were as follows: δ 6.70 (d, 1H, J=9Hz, H-4), ca. 6.80-9.00 (D2O-exchangeable broad peak, 2H, NH2), 7.66 (d, 1H, J=9Hz, H-5), and 7.93 (s, 1H, H-3). The mass spectrum (70 eV) showed molecular ion peaks m/e 177 (100%, M+) and m/e 159 (86%, M+-H2O). Samples recrystallized from methanol failed to yield satisfactory data by elemental analysis.

References

[1] Tetrahedron Letters, 1980, vol. 21, # 32, p. 3029 - 3032
[2] Journal of Organic Chemistry, 1980, vol. 45, # 15, p. 3072 - 3077
[3] Heterocycles, 1981, vol. 15, # 2, p. 1053 - 1059
[4] Patent: US4223143, 1980, A
[5] Patent: WO2007/93402, 2007, A1. Location in patent: Page/Page column 42

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