| Identification | Back Directory | [Name]
2,3-Dihydro-1H-Pyrrolo[3,4-C]Pyridine dihydrochloride | [CAS]
6000-50-6 | [Synonyms]
Dihydrochlorid
2,3-Dihydro-1H-pyrroL
o[3,4-c]pyridine DihydrochL
2,3-Dihydro-1H-pyrrolo[3,4-c]pyridin
2,3-Dihydro-1H-pyrrolo[3,4-c]pyridine 2HCl
2,3-dihydro-1H-pyrrolo[3,4-c]pyridine diHCl
1H,2H,3H-pyrrolo[3,4-c]pyridine dihydrochloride
2,3-DIHYDRO-1H-PYRROLO[3,4-C]PYRIDINE HYDROCHLO
2,3-Dihydro-1H-Pyrrolo[3,4-C]Pyridine dihydrochloride
2,3-Dihydro-1H-Pyrrolo[3,5-C]Pyridine dihydrochloride
2,3-dihydro-1H-pyrrolo[3,4-c]pyridine dihydrogen chloride
2,3-Dihydro-1H-Pyrrolo[3,4-C]Pyridine dihydrochloride ISO 9001：2015 REACH | [EINECS(EC#)]
201-525-2 | [Molecular Formula]
C7H10Cl2N2 | [MDL Number]
MFCD15144657 | [MOL File]
6000-50-6.mol | [Molecular Weight]
193.074 |
| Questions And Answer | Back Directory | [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. |
| Hazard Information | Back Directory | [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 undergoe |
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SynAsst Chemical.
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021-60343070 |
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Chem-Stone Co.,Ltd.
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Cool Pharm, Ltd
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