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Chemical Structure| 135207-17-9 Chemical Structure| 135207-17-9

Structure of 135207-17-9

Chemical Structure| 135207-17-9

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Product Details of [ 135207-17-9 ]

CAS No. :135207-17-9
Formula : C6H8N2
M.W : 108.14
SMILES Code : N1(C2CC2)C=CN=C1
MDL No. :MFCD22690770
InChI Key :LMUSCNPAUSJVDG-UHFFFAOYSA-N
Pubchem ID :10034603

Safety of [ 135207-17-9 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H320-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 135207-17-9 ]

* 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 [ 135207-17-9 ]

[ 135207-17-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 135207-17-9 ]
  • [ 1262035-61-9 ]
YieldReaction ConditionsOperation in experiment
37% With 1,3-dibromo-5,5-dimethylimidazolidine-2,4-dione; In dichloromethane; at 5 - 10℃; for 2h; Step 2 Cyclopropyl-1H-imidazole (1.18 g, 10.9 mmol) was dissolved in methylene chloride (0.1 M), cooled to 5-10 C., and 1,3-dibromo-5,5-dimethylhydantoin (1.59 g, 5.57 mmol) was added. The temperature was maintained between 5-10 C. and the reaction was stirred for 2 hours. Solvent was removed from the reaction mixture under reduced pressure, and the residue was purified by column chromatography (eluding with 1%-7% methanol in methylene chloride, 5% methanol/methylene chloride) to afford 620 mg (37% yield) of 5-bromo-1-cyclopropyl-1H-imidazole.
1.21 g With 1,3-dibromo-5,5-dimethylimidazolidine-2,4-dione; In dichloromethane; at 5℃; Intermediate lc' 5-Bromo- 1-cyclopropyl- lH-imidazole In a 350 mL four-necked flask, 1-cyclopropyl- lH-imidazole (2.58 g, 23.9 mmol, Eq: 1.00) was combined with DCM (100 ml) to give a colorless solution. l,3-Dibromo-5,5- dimethylimidazolidine-2,4-dione (3.48 g, 12.2 mmol, Eq: 0.51), dissolved in dichloromethane (100 ml) was added drop wise at 5C and the reaction mixture stirred at 5C for 2.5hr. Work up: The reaction mixture was quenched with 100ml Na2S03 sol. and extracted with DCM (2X200ml). The organic layers were washed with H20/NaCl sol, dried over Na2S04 and concentrated i. V. The crude product was purified by flash chromatography (silica gel, 120g, 25% to 100% EtOAc in heptane) to give 1.21g of the title compound as colorless oil. MS (ESI): 187.9/189.1 [M+H]+.
1.21 g With 1,3-dibromo-5,5-dimethylimidazolidine-2,4-dione; In dichloromethane; at 5℃; for 2.5h;Inert atmosphere; In a 350 mL four-necked flask, 1-cyclopropyl-1H-imidazole (2.58 g, 23.9 mmol, Eq: 1.00) was combined with DCM (100 ml) to give a colorless solution. 1,3-Dibromo-5,5-dimethylimidazolidine-2,4-dione (3.48 g, 12.2 mmol, Eq: 0.51), dissolved in dichloromethane (100 ml) was added dropwise at 5 C. and the reaction mixture stirred at 5 C. for 2.5 hr. Work up: The reaction mixture was quenched with 100 ml Na2SO3 sol. and extracted with DCM (2*200 ml). The organic layers were washed with H2O/NaCl sol, dried over Na2SO4 and concentrated i. V. The crude product was purified by flash chromatography (silica gel, 120 g, 25% to 100% EtOAc in heptane) to give 1.21 g of the title compound as colorless oil. MS (ESI): 187.9/189.1 [M+H]+.
 

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