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Chemical Structure| 144288-48-2 Chemical Structure| 144288-48-2

Structure of 144288-48-2

Chemical Structure| 144288-48-2

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Product Details of [ 144288-48-2 ]

CAS No. :144288-48-2
Formula : C6H9N3
M.W : 123.16
SMILES Code : NC1=NC=CC=C1CN
MDL No. :MFCD06213856
InChI Key :MSEQBCDSEVCGDC-UHFFFAOYSA-N
Pubchem ID :12358233

Safety of [ 144288-48-2 ]

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

Application In Synthesis of [ 144288-48-2 ]

* 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 [ 144288-48-2 ]

[ 144288-48-2 ] Synthesis Path-Downstream   1~1

  • 1
  • (PhO)2PON3 [ No CAS ]
  • [ 39067-29-3 ]
  • [ 144288-48-2 ]
  • 1-(3-Amino-pyridin-2-yl)-3-(2-pyridin-3-yl-thiazol-4-yl)-urea [ No CAS ]
YieldReaction ConditionsOperation in experiment
With triethanolamine;silica gel; In tetrahydrofuran; EXAMPLE 229 1-(3-Amino-pyridin-2-yl)-3-(2-pyridin-3-yl-thiazol-4-yl)-urea TEA (0.27 mL, 1.94 mmol) was added to a solution of <strong>[39067-29-3]2-(pyridin-3-yl)thiazole-4-carboxylic acid</strong> (200 mg, 0.97 mmol) and 4A molecular sieves in THF (25 mL) under N2 at RT. (Pho)2PON3 (0.33 mL, 1.55 mmol) followed by 2-amino-3-aminomethylpyridine (265 mg, 2.43 mmol) was added and the resulting mixture was heated at reflux for 12 h. After cooling to RT, the heterogeneous mixture was decanted to remove the molecular sieves. The precipitate was collected and discarded. The filtrate was purified by chromatography on silica gel (CH2Cl2/MeOH, 95:5) to give a white solid. MS m/z: 313.8 (M+H). Calc'd for C14H12N6OS-312.36.
With triethanolamine;silica gel; In tetrahydrofuran; EXAMPLE 229 1-(3-Amino-pyridin-2-yl)-3-(2-pyridin-3-yl-thiazol-4-yl)-urea TEA (0.27 mL, 1.94 mmol) was added to a solution of <strong>[39067-29-3]2-(pyridin-3-yl)thiazole-4-carboxylic acid</strong> (200 mg, 0.97 mmol) and 4A molecular sieves in THF (25 mL) under N2 at RT. (PhO)2PON3 (0.33 mL, 1.55 mmol) followed by 2-amino-3-aminomethylpyridine (265 mg, 2.43 mmol) was added and the resulting mixture was heated at reflux for 12 h. After cooling to RT, the heterogeneous mixture was decanted to remove the molecular sieves. The precipitate was collected and discarded. The filtrate was purified by chromatography on silica gel (CH2Cl2/MeOH, 95:5) to give a white solid. MS m/z: 313.8 (M+H). Calc'd for C14H12N6OS-312.36.
 

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