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Chemical Structure| 1224719-40-7 Chemical Structure| 1224719-40-7

Structure of 1224719-40-7

Chemical Structure| 1224719-40-7

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Product Details of [ 1224719-40-7 ]

CAS No. :1224719-40-7
Formula : C9H11NO2
M.W : 165.19
SMILES Code : OC1=CC=C(OCC2CC2)N=C1
MDL No. :MFCD28128936

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Application In Synthesis of [ 1224719-40-7 ]

* 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 [ 1224719-40-7 ]

[ 1224719-40-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 34368-52-0 ]
  • [ 1224719-40-7 ]
  • [ 1593700-31-2 ]
YieldReaction ConditionsOperation in experiment
With di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; dichloromethane; at 30℃; for 12h; (R)-3-[6-(2-Cyclopropyl-methoxy)-pyridin-3-yloxy]-pyrrolidin-2-one A mixture of (S)-3-hydroxy-pyrrolidin-2-one (3.00 g), 6-(2-cyclopropyl-methoxy)-pyridin-3-ol (4.90 g), triphenylphosphine (polymer, 8.56 g), DCM (30 mL) and THF (50 mL) was added DIAD (6.60 g) keeping the reaction temperature below 30° C. After 12 hours the mixture was filtered and the filtrate was evaporated. The residue was purified by SGC (eluent: EA/MeOH 9:1) to provide the title compound. MS ESI+: m/z=249 [M+H]+.
With di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; dichloromethane; at 30℃; for 12h; A mixture of (S)-3-hydroxy-pyrrolidin-2-one (3.00 g), 6-(2-cyclopropyl-methoxy)-pyridin- 3-ol (4.90 g), triphenylphosphine (polymer, 8.56 g), DCM (30 mL) and THF (50 mL) was added DIAD (6.60 g) keeping the reaction temperature below 30°C. After 12 hours the mixture was filtered and the filtrate was evaporated. The residue was purified by SGC (eluent: EA MeOH 9:1 ) to provide the title compound. MS ESI+: m/z = 249 [M+H]+.
With triphenylphosphine on polystyrene; di-isopropyl azodicarboxylate; In tetrahydrofuran; dichloromethane; at 30℃; for 12h; To a mixture of (S)-3-hydroxy-pyrrolidin-2-one (3.00 g), 6-(2-cyclopropyl-methoxy)- pyridin-3-ol (4.90 g), triphenylphosphine (polymer, 8.56 g), DCM (30 mL) and THE (50 mL) was added DIAD (6.60 g) keeping the reaction temperature below 30°C. After 12hours the mixture was filtered and the filtrate was evaporated. The residue was purified by SGC (eluent: EAIMeOH 9:1) to provide the title compound. MS ESI: mlz = 249 [M+H].
With di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; dichloromethane; at 30℃; for 12h; (R)-3-[6-(2-Cyclopropyl-methoxy)-pyridin-3-yloxy]-pyrrolidin-2-one A mixture of (S)-3-hydroxy-pyrrolidin-2-one (3.00 g), 6-(2-cyclopropyl-methoxy)-pyridin- 3-ol (4.90 g), triphenylphosphine (polymer, 8.56 g), DCM (30 mL) and THF (50 mL) was added DIAD (6.60 g) keeping the reaction temperature below 30°C. After 12 hours the mixture was filtered and the filtrate was evaporated. The residue was purified by SGC (eluent: EA MeOH 9:1 ) to provide the title compound. MS ESI+: m/z = 249 [M+H]+.
With di-isopropyl azodicarboxylate; In tetrahydrofuran; dichloromethane; at 30℃; for 12h; A mixture of (S)-3-hydroxy-pyrrolidin-2-one (3.00 g), 6-(2-cyclopropyl-methoxy)-pyridin-3-01 (4.90 g), triphenylphosphine (polymer, 8.56 g), DCM (30 mL) and THF (50 mL) was added DIAD (6.60 g) keeping the reaction temperature below 30° C. After 12 hours, the mixture was filtered and the filtrate was evaporated. The residue was purified by SGC (eluent: EA/MeOH 9:1) to provide (R)-3-[6-(2-cyclopropyl-methoxy)-pyridin-3-yloxy]-pyrrolidin-2-one. MS ESI+: m/z=249 [M+H]+.

 

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