Basic information Safety Supplier Related

7H-Pyrazolo[4,3-d]pyrimidin-7-one, 1,4-dihydro-1-methyl- (9CI)

Basic information Safety Supplier Related

7H-Pyrazolo[4,3-d]pyrimidin-7-one, 1,4-dihydro-1-methyl- (9CI) Basic information

Product Name:
7H-Pyrazolo[4,3-d]pyrimidin-7-one, 1,4-dihydro-1-methyl- (9CI)
Synonyms:
  • 7H-Pyrazolo[4,3-d]pyrimidin-7-one, 1,4-dihydro-1-methyl- (9CI)
  • 1-Methyl-1H-pyrazolo[4,3-d]pyriMidin-7-ol
  • 1-Methyl-1,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one
  • 1,6-dihydro-1-methyl-7H-Pyrazolo[4,3-d]pyrimidin-7-one
  • 7H-Pyrazolo[4,3-d]pyrimidin-7-one, 1,6-dihydro-1-methyl-
CAS:
314021-93-7
MF:
C6H6N4O
MW:
150.14
Product Categories:
  • PYRIMIDINE
Mol File:
314021-93-7.mol
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7H-Pyrazolo[4,3-d]pyrimidin-7-one, 1,4-dihydro-1-methyl- (9CI) Chemical Properties

storage temp. 
2-8°C
Appearance
White to off-white Solid
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7H-Pyrazolo[4,3-d]pyrimidin-7-one, 1,4-dihydro-1-methyl- (9CI) Usage And Synthesis

Synthesis

923283-54-9

3473-63-0

314021-93-7

GENERAL STEPS: To a mixture of 4-amino-1-methyl-1H-pyrazole-5-carboxylic acid methyl ester (0.92 g, 5.9 mmol) dissolved in 5 mL of a mixture of N,N-diisopropylethylamine (Hunig base) and 5 mL of n-butanol was added formamidine acetate (0.68 g, 6.5 mmol). The reaction mixture was heated to 110 °C and stirred for 1 hour. After completion of the reaction, it was cooled to room temperature, the white precipitate was collected by filtration and washed with ether. The resulting white solid was dried under reduced pressure to afford 1-methyl-1H-pyrazolo[4,3-d]pyrimidin-7-ol (0.83 g, 94% yield). The product was characterized by 1H NMR (d6-DMSO): δ 4.33 (s, 3H), 8.50 (s, 1H), 8.80 (s, 1H); electrospray mass spectrometry (ES-MS) showed m/e = 151 ([M + H]+).

References

[1] Patent: US2007/27166, 2007, A1. Location in patent: Page/Page column 80

7H-Pyrazolo[4,3-d]pyrimidin-7-one, 1,4-dihydro-1-methyl- (9CI)Supplier

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