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Chemical Structure| 7148-07-4 Chemical Structure| 7148-07-4

Structure of 7148-07-4

Chemical Structure| 7148-07-4

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Product Details of [ 7148-07-4 ]

CAS No. :7148-07-4
Formula : C9H15N
M.W : 137.22
SMILES Code : N1(C2=CCCC2)CCCC1
MDL No. :MFCD00003162
InChI Key :KOFSFYBXUYHNJL-UHFFFAOYSA-N
Pubchem ID :81570

Safety of [ 7148-07-4 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 7148-07-4 ]

* 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 [ 7148-07-4 ]

[ 7148-07-4 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 7148-07-4 ]
  • [ 39777-61-2 ]
  • [ 67860-98-4 ]
  • [ 89725-77-9 ]
  • 2
  • [ 7148-07-4 ]
  • [ 114078-88-5 ]
  • 3-bromo-6,7-dihydro-5H-cyclopenta[b]pyridine [ No CAS ]
YieldReaction ConditionsOperation in experiment
36% In chloroform; at 45℃; for 1.0h; To a solution of <strong>[114078-88-5]5-bromo-1,2,3-triazine</strong> (25 g, 156 mmol, 1.0 equiv) in CHCl3 (500 mL) was added 1-(cyclopent-1-en-1-yl)pyrrolidine (25.8 g, 188 mmol, 1.1 equiv). The mixture was stirred at 45 oC for 1 h, diluted with DCM (500 mL), washed with brine (300 mL) twice, dried over anhydrous sodium sulfate, concentrated under reduced pressure, and purified by silica gel chromatography (EA/PE, 10/90) to give 11 g (36%) of 3-bromo- 5H,6H,7H-cyclopenta[b]pyridine as a brown solid.
34.2% In chloroform; at 0 - 45℃; for 0.833333h; Weigh <strong>[114078-88-5]5-bromo-1,2,3-triazine</strong> (4.4g, 27.5mmol) was dissolved in chloroform (40 mL), and cooled to 0 deg.] C, was added 1-(cyclopentan-1-en-1-yl)pyrrolidine with stirring -1 After the addition, the reaction mixture was stirred at 0 C for 5 minutes, and raised to 45 C for 45 minutes. The crude product was purified by column chromatography on silica gel (petroleum ether: ethyl acetate = 5: 1 (1: 1) ) to give the title compound (1.86g, yield 34.2%).
34.3% In chloroform; at 45℃; for 16.0h; To a solution of compound S3 (400 mg, 2.5 mmol) in CHCl3(10 mL) was added 1-(cyclopent-1-en-1-yl)pyrrolidine (516 mg, 3.8 mmol). The reaction was stirred at 45 C. for 16 hrs. The reaction mixture was diluted with DCM and washed water, brine, dried over anhydrous Na2SO4, filtered, and concentrated. The residue was purified by silica gel column (eluted with EtOAc/PE=1/10) to give the title compound (170 mg, 34.3% yield) as a gray solid.
 

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