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Chemical Structure| 558478-81-2 Chemical Structure| 558478-81-2

Structure of 558478-81-2

Chemical Structure| 558478-81-2

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Product Details of [ 558478-81-2 ]

CAS No. :558478-81-2
Formula : C7H14ClN
M.W : 147.65
SMILES Code : [H]Cl.C1(C2CC2)NCCC1
MDL No. :MFCD11841135
InChI Key :OJKJZUXVQAPXRU-UHFFFAOYSA-N
Pubchem ID :50988052

Safety of [ 558478-81-2 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 558478-81-2 ]

* 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 [ 558478-81-2 ]

[ 558478-81-2 ] Synthesis Path-Downstream   1~5

  • 2
  • [ 1227910-60-2 ]
  • [ 558478-81-2 ]
YieldReaction ConditionsOperation in experiment
With hydrogenchloride; hydrogen;palladium 10% on activated carbon; In ethanol; water; at 20.0℃;Inert atmosphere; Intermediate 57; 2-Cvclopropylpyrrolidine; To a solution of 2-cyclopropyl-1-(phenylmethyl)pyrrolidine (100 mg, 0.50 mmol) in ethanol (5 ml.) was added 1 N HCI(aq) (0.50 ml_, 0.50 mmol), and the resulting mixture was purged with N2 for 10 minutes. Pd/C (10 mg, 10 wt%) was added and the reaction mixture was stirred overnight at room temperature under a H2 atmosphere (balloon setup). LCMS analysis indicated -20% desired product and -70% starting material. More Pd/C was added (30 mg), and the reaction mixture was stirred under a H2 atmosphere for an additional 24 hours. Additional 1 N HCI(aq) (0.50 ml_, 0.50 mmol) was added, and the mixture was filtered through an Acrodisk, washing with ethanol. The solution was evaporated, and the resulting residue was triturated with diethyl ether to afford the HCI salt of the title compound (74 mg) as a white solid. 1H NMR (400 MHz, CD3OD): δ 0.37 - 0.54 (m, 2H), 0.67 - 0.80 (m, 2H), 0.98 - 1.15 (m, 1 H), 1.77 - 1.93 (m, 1 H), 1.96 - 2.18 (m, 2H), 2.18 - 2.30 (m, 1 H), 2.84 - 2.98 (m, 1 H), 3.20 - 3.30 (m, 1 H), 3.30 - 3.43 (m, 1 H).
To a solution of 2-cyclopropyl-1-(phenylmethyl)pyrrolidine (100 mg, 0.50 mmol) in ethanol (5 mL) was added 1 N HCI(aq) (0.50 mL, 0.50 mmol), and the resulting mixture was purged with N2 for 10 minutes. Pd/C (10 mg, 10 wt%) was added and the reaction mixture was stirred overnight at room temperature under a H2 atmosphere (balloon setup). LCMS analysis indicated -20% desired product and -70% starting material. More Pd/C was added (30 mg), and the reaction mixture was stirred under a H2 atmosphere for an additional 24 hours. Additional 1 N HCI(aq) (0.50 mL, 0.50 mmol) was added, and the mixture was filtered through an Acrodisk, washing with ethanol. The solution was evaporated, and the resulting residue was triturated with diethyl ether to afford the HCI salt of the title compound (74 mg) as a white solid. 1H NMR (400 MHz, CD3OD): δ 0.37 - 0.54 (m, 2H), 0.67 - 0.80 (m, 2H), 0.98 - 1.15 (m, 1 H), 1.77 - 1.93 (m, 1 H), 1.96 - 2.18 (m, 2H), 2.18 - 2.30 (m, 1 H), 2.84 - 2.98 (m, 1 H), 3.20 - 3.30 (m, 1 H), 3.30 - 3.43 (m, 1 H).
  • 3
  • [ 558478-81-2 ]
  • [ 3383-21-9 ]
  • 5-cyclopropyl-1-(3,5-di-tert-butyl-2-hydroxyphenyl)pyrrolidin-2-one [ No CAS ]
  • 4
  • [ 558478-81-2 ]
  • [ 3383-21-9 ]
  • 5,7-Ditert-butyl-1-cyclopropyl-1,2,3,3a-tetrahydrobenzo[d]pyrrolo[2,1-b]-oxazole [ No CAS ]
  • 5
  • 2,4-di-tert-butyl-6-(2-cyclopropylpyrrolidin-1-yl)phenol [ No CAS ]
  • [ 558478-81-2 ]
  • [ 3383-21-9 ]
 

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