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Chemical Structure| 124458-11-3 Chemical Structure| 124458-11-3

Structure of 124458-11-3

Chemical Structure| 124458-11-3

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Product Details of [ 124458-11-3 ]

CAS No. :124458-11-3
Formula : C8H11N3OS
M.W : 197.26
SMILES Code : CC(N1CCC2=C(SC(N)=N2)C1)=O
MDL No. :MFCD10010939
InChI Key :FNPABBLKLMLVLD-UHFFFAOYSA-N
Pubchem ID :15017650

Safety of [ 124458-11-3 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of [ 124458-11-3 ]

* 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 [ 124458-11-3 ]

[ 124458-11-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 124458-11-3 ]
  • [ 97817-23-7 ]
YieldReaction ConditionsOperation in experiment
With sodium hydroxide; ammonium chloride; In ethanol; chloroform; 2. 2-Amino-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridine 5-Acetyl-2-amino-4,5,6,7-tetrahydrothiazolo-[5,4-c]pyridine (110 mg, 0.51 mmol) was dissolved in ethanol (1 ml) and treated with sodium hydroxide (15.4 mg, 0.38 mmol) in ethanol (1 ml). The solution was heated to 100 for 16 hours, then treated with additional sodium hydroxide (25.6 mg, 0.64 mmol) and heated to reflux for an additional 16 hours. Solid ammonium chloride was added, and the mixture was filtered and concentrated in vacuo. The residue was dissolved in chloroform, dried over sodium sulfate and solvent was removed, leaving the title product (67.4 mg, 0.43 mmol, 84% yield) as a yellow solid, which was used without further purification.
 

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