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Chemical Structure| 30720-25-3 Chemical Structure| 30720-25-3

Structure of 30720-25-3

Chemical Structure| 30720-25-3

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Product Details of [ 30720-25-3 ]

CAS No. :30720-25-3
Formula : C11H12ClN3O2
M.W : 253.69
SMILES Code : O=C(C1=CN=C(N(CC)N=C2)C2=C1Cl)OCC
MDL No. :MFCD06656752

Safety of [ 30720-25-3 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis of [ 30720-25-3 ]

* 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 [ 30720-25-3 ]

[ 30720-25-3 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 33024-60-1 ]
  • [ 30720-25-3 ]
  • [ 675112-01-3 ]
YieldReaction ConditionsOperation in experiment
Intermediate 1 (2. [5G)] was dissolved in acetonitrile [(15ML).] 4-Aminotetrahydropyran hydrochloride [(1.] [LG)] and N, N-diisopropylethylamine (9. [4ML)] were added and the mixture stirred under nitrogen at [85°C] for 16h. A trace of starting material remained, so an additional portion of 4-aminotetrahydropyran hydrochloride [(O.] [L] lg) was added and stirring continued at [85°C] for a further [16H.] The mixture was then concentrated in vacuo. The residue was partitioned between DCM and water. The layers were separated and the organic layer was washed with further water [(2X20ML)] then dried [(NA2S04)] and concentrated in vacuo. The residue was further purified by chromatography using Biotage (silica, 90g), eluting with cyclohexane: ethyl acetate to afford Example 3 (2.45g). LCMS showed MH+ [= 319] ; TRET = 2. [90MIN.]
  • 2
  • [ 214147-48-5 ]
  • [ 30720-25-3 ]
  • ethyl 4-[(1-acetyl-4-piperidinyl)amino]-1-ethyl-1H-pyrazolo[3,4-b]pyridine-5-carboxylate [ No CAS ]
YieldReaction ConditionsOperation in experiment
With N-ethyl-N,N-diisopropylamine; In acetonitrile; at 85℃; for 34h; Intermediate 1 (2.58g), Intermediate 6 (2. [0G)] and N, N-diisopropylethylamine (8. [9ML)] were dissolved in acetonitrile (98ml). The reaction mixture was heated at [85 C] for 24h then an additional portion of Intermediate 6 (0. [18G)] was added and heating continued for a further [L OH.] The reaction was concentrated in vacuo and the residues partitioned between DCM and water. The phases were separated and the organic phase evaporated in vacuo. The residue was purified by chromatography using Biotage (silica 90g) eluting with DCM: MeOH (5%) to afford Example 207 [(1.] 55g) as a white solid. LCMS showed MH+ 360; TROT= 2.71 min.
  • 3
  • [ 30720-25-3 ]
  • [ 94-98-4 ]
  • [ 865718-72-5 ]
 

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