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Chemical Structure| 134574-96-2 Chemical Structure| 134574-96-2

Structure of 134574-96-2

Chemical Structure| 134574-96-2

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Product Details of [ 134574-96-2 ]

CAS No. :134574-96-2
Formula : C11H20N2O2
M.W : 212.29
SMILES Code : O=C(OC(C)(C)C)NCC12CNCC1C2
MDL No. :MFCD11035741
InChI Key :UIYMGRQQGQOESZ-UHFFFAOYSA-N
Pubchem ID :15713426

Safety of [ 134574-96-2 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P280-P305+P351+P338

Application In Synthesis of [ 134574-96-2 ]

* 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 [ 134574-96-2 ]

[ 134574-96-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 134574-96-2 ]
  • [ 93107-30-3 ]
  • [ 134575-56-7 ]
YieldReaction ConditionsOperation in experiment
79% With triethylamine; In acetonitrile; A. 7-{1-[(N-tert-Butoxycarbonyl)aminomethyl]-3-azabicyclo[3.1.0]hex-3-yl}-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-quinoline-3-carboxylic acid A mixture of 1-[(N-tert-butoxycarbonyl)aminomethyl]-3-azabicyclo[3.1.0]hexane (0.30 g, 1.41 mmol) and triethylamine (0.39 ml, 2.8 mmol) in acetonitrile (20 ml) was treated with 1-cyclopropyl-6,7-difluoro-1,4-dihydro-4-oxo-quinoline-3-carboxylic acid (0.375 g, 1.41 mmol) and heated to 50° for 21 hours. The temperature was then increased to 80° for 24 hours. Filtration of the reaction mixture then provided the title product as a white solid, mp 235.5°-236° (508 mg, 1.11 mmol, 79percent yield). 1 H NMR (CDCl3/ CD3 OD): 8.62 (s, 1H), 7.84 (d, J=14 Hz, 1H), 6.88 (d, J=7 Hz, 1H), 5.06 (vbs, 1H), 3.84 (m, 2H), 3.68 (m, 1H), 3.58 (m, 1H), 3.48 (m, 1H), 3.36(bs, 2H), 1.64 (m, 1H), 1.45 (s, 9H), 1.36 (m, 2H), 1.17 (m, 2H), 0.87 (m, 1H), 0.66 (m, 1H).
79% With triethylamine; In acetonitrile; A. 7-{1-[(N-tert-Butoxycarbonyl)aminomethyl]-3-azabicyclo[3.1.0]hex-3-yl}-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-quinoline-3-carboxylic acid A mixture of 1-[(N-tert-butoxycarbonyl)aminomethyl]-3-azabicyclo[3.1.0]hexane (0.30 g, 1.41 mmol) and triethylamine (0.39 ml, 2.8 mmol) in acetonitrile (20 ml) was treated with 1-cyclopropyl-6,7-difluoro-1,4-dihydro-4-oxo-quinoline-3-carboxylic acid (0.375 g, 1.41 mmol) and heated to 50° for 21 hours. The temperature was then increased to 80° for 24 hours. Filtration of the reaction mixture then provided the title product as a white solid, mp 235.5-236° (508 mg, 1.11 mmol, 79percent yield). 1H NMR (CDCl3/CD3OD): 8.62 (s, 1H), 7.84 (d, J=14 Hz, 1H), 6.88 (d, J=7 Hz, 1H), 5.06 (vbs, 1H), 3.84 (m, 2H), 3.68 (m, 1H), 3.58 (m, 1H), 3.48 (m, 1H), 3.36 (bs, 2H), 1.64 (m, 1H), 1.45 (s, 9H), 1.36 (m, 2H), 1.17 (m, 2H), 0.87 (m, 1H), 0.66 (m, 1H).
 

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