2,3-Dihydro-1H-Pyrrolo[3,4-C]Pyridine dihydrochloride
2,3-Dihydro-1H-Pyrrolo[3,4-C]Pyridine dihydrochloride Basic information
- Product Name:
- 2,3-Dihydro-1H-Pyrrolo[3,4-C]Pyridine dihydrochloride
- Synonyms:
-
- 2,3-Dihydro-1H-Pyrrolo[3,4-C]Pyridine dihydrochloride
- 2,3-Dihydro-1H-pyrrolo[3,4-c]pyridine 2HCl
- 2,3-Dihydro-1H-Pyrrolo[3,5-C]Pyridine dihydrochloride
- 2,3-dihydro-1H-pyrrolo[3,4-c]pyridine diHCl
- 2,3-Dihydro-1H-pyrrolo[3,4-c]pyridin
- Dihydrochlorid
- 1H,2H,3H-pyrrolo[3,4-c]pyridine dihydrochloride
- 2,3-DIHYDRO-1H-PYRROLO[3,4-C]PYRIDINE HYDROCHLO
- CAS:
- 6000-50-6
- MF:
- C7H9ClN2
- MW:
- 156.61
- EINECS:
- 201-525-2
- Mol File:
- 6000-50-6.mol
2,3-Dihydro-1H-Pyrrolo[3,4-C]Pyridine dihydrochloride Chemical Properties
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- Appearance
- Off-white to gray Solid
2,3-Dihydro-1H-Pyrrolo[3,4-C]Pyridine dihydrochloride Usage And Synthesis
Application
2,3-Dihydro-1H-pyrrole[3,4-C]pyridine dihydrochloride can be used as a pharmaceutical synthesis intermediate and can be prepared from propargylamine and ethyl chloroformate through a four-step reaction. Literature reports its potential use in the preparation of an A2A receptor antagonist.
Synthesis
a. Propargylamine reacts with ethyl chloroformate to give ethyl N-propargylcarbamate.
b. The product from step a reacts with 2-chloromethylpyrimidine to yield 2-(N-ethoxycarbonyl-N-propargylaminomethyl)pyrimidine.
c. The product from step b undergoes cyclization by refluxing in xylene to give ethyl 5,7-dihydro-6H-pyrrolo[3,4-b]pyridine-6-carboxylate.
d. The ester from step c is hydrolyzed/decarboxylated in conc. HCl to yield 2,3-dihydro-1H-pyrrolo[3,4-c]pyridine dihydrochloride.
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