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Chemical Structure| 35018-15-6 Chemical Structure| 35018-15-6

Structure of 35018-15-6

Chemical Structure| 35018-15-6

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Product Citations

Product Citations

Wang, Feijun ; Frankowski, Kevin J. ;

Abstract: We developed an electrochemical carboamidation sequence that affords either cyclic β-amidoamine products via direct functionalization or linear hydroxybisamide products via a ring opening pathway. The reaction pathway was dependent on the nature of the N-acyl activating group, with carbamate groups favoring direct isocyanide addition to the N-acyliminium ion intermediate and the benzoyl activating group favoring the ring opening–functionalization pathway. Both protocols are one-pot reaction sequences, have general applicability, and lead to peptide-like products of greatly increased molecular complexity.

Alternative Products

Product Details of [ 35018-15-6 ]

CAS No. :35018-15-6
Formula : C6H13N
M.W : 99.17
SMILES Code : CC1(C)NCCC1
MDL No. :MFCD08457313
InChI Key :PHODFIDDEBEGCS-UHFFFAOYSA-N
Pubchem ID :414773

Safety of [ 35018-15-6 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H302+H312+H332-H314
Precautionary Statements:P280-P305+P351+P338-P310
Class:8
UN#:2735
Packing Group:

Application In Synthesis of [ 35018-15-6 ]

* 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 [ 35018-15-6 ]

[ 35018-15-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 35018-15-6 ]
  • [ 1597-32-6 ]
  • [ 1431773-89-5 ]
YieldReaction ConditionsOperation in experiment
4% In water; at 205℃; for 0.5h;Sealed tube; Microwave irradiation; A mixture of <strong>[1597-32-6]6-fluoropyridin-2-amine</strong> (0.5 g, 4.46 mmol) and 2,2-dimethylpyrrolidine (0.67 g, 6.75 mmol) in water (0.3 mL) was heated to 205 C. for 0.5 h in a sealed tube in a microwave oven then concentrated in vacuo. The residue was purified by chromatography (silica gel, 10 g, 200˜300 mesh, ethyl acetate:petroleum ether=1:15) to afford 6-(2,2-dimethylpyrrolidin-1-yl)pyridin-2-amine (0.035 g, 4%) as a yellow oil. LC-MS: [M+1]+=192, tR=1.048 min.
4% In water; at 205℃; for 0.5h;Microwave irradiation; Sealed tube; A mixture of <strong>[1597-32-6]6-fluoropyridin-2-amine</strong> (0.5 g, 4.46 mmol) and 2,2-dimethylpyrrolidine (0.67 g, 6.75 mmol) in water (0.3 mL) was heated to 205 C for 0.5 h in a sealed tube in a microwave oven then concentrated in vacuo. The residue was purified by chromatography (silica gel, 10 g, 200 ~ 300 mesh, ethyl acetate : petroleum ether = 1 : 15 ) to afford 6-(2,2-dimethylpyrrolidin-l- yl) pyridin-2-amine (0.035 g, 4 %) as a yellow oil. LC-MS: [M + l]+ = 192 > tR = 1.048min.
 

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