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Chemical Structure| 888498-07-5 Chemical Structure| 888498-07-5

Structure of 4-Aminomethyl-7-azaindole
CAS No.: 888498-07-5

Chemical Structure| 888498-07-5

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Product Details of [ 888498-07-5 ]

CAS No. :888498-07-5
Formula : C8H9N3
M.W : 147.18
SMILES Code : NCC1=C2C(NC=C2)=NC=C1
MDL No. :MFCD08458223
InChI Key :KPNRVZRVBULYGJ-UHFFFAOYSA-N
Pubchem ID :11679841

Safety of [ 888498-07-5 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H332-H335
Precautionary Statements:P280-P305+P351+P338-P310

Application In Synthesis of [ 888498-07-5 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 888498-07-5 ]

[ 888498-07-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 888498-07-5 ]
  • [ 171178-50-0 ]
  • [ 935466-87-8 ]
YieldReaction ConditionsOperation in experiment
In a 100 ml RBF were combined <strong>[171178-50-0]2,6-difluoronicotinic acid</strong> (1.47 g, 9.24 mmol), (IH- pyrrolo[2,3-]pyridin-4-yl)methanamine (1.36 g, 9.24 mmol), DIEA (2.39 g, 18.48 mmol), and TηF (35 ml). The mix was heated at 80 0C for 9 h. A beige solid was removed by filtration. The filtrate was concentrated under vacuum and then treated with CH2Cl2 to yield more beige solid, which was also isolated by filtration. The two batches of beige solid were combined and dissolved into 1 NNaOH (aq). The aqueous solution was extracted once with CH2Cl2 and then with EtOAc before being acidified to pH 4.5. The ensuing yellow precipitate was isolated by filtration and dried under vacuum to yield the titled compound.
 

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[ 888498-07-5 ]

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