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Chemical Structure| 190900-22-2 Chemical Structure| 190900-22-2

Structure of 190900-22-2

Chemical Structure| 190900-22-2

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Product Details of [ 190900-22-2 ]

CAS No. :190900-22-2
Formula : C11H20N2O3
M.W : 228.29
SMILES Code : O=C(N1CCN=C(OC)CC1)OC(C)(C)C

Safety of [ 190900-22-2 ]

Application In Synthesis of [ 190900-22-2 ]

* 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 [ 190900-22-2 ]

[ 190900-22-2 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 420-37-1 ]
  • [ 190900-21-1 ]
  • [ 190900-22-2 ]
YieldReaction ConditionsOperation in experiment
180 mg (85%) In dichloromethane; ethyl acetate; Step C 1-(tert-Butoxycarbonyl)-2,3,6,7-tetrahydro-5-methoxy-(1H)-1,4-diazepine Trimethyloxonium tetrafluoroborate (Meerwein's salt) (141 mg, 0.94 mmol) was added in one portion to a solution of <strong>[190900-21-1]1-(tert-butoxycarbonyl)hexahydro-(5H)-1,4-diazepin-5-one</strong> (200 mg, 0.94 mmol) in 2.0 mL of anhydrous methylene chloride. The mixture was stirred overnight at room temperature. The reaction mixture was partitioned between 10 mL of saturated aqueous sodium bicarbonate and 20 mL of ethyl acetate. The organic layer was separated and the aqueous layer was extracted with 3*10 mL of ethyl acetate. The combined ethyl acetate layers were washed with saturated aqueous sodium bicarbonate and saturated aqueous sodium chloride. After drying over anhydrous sodium sulfate, the organic solution was concentrated in vacuo to give 180 mg (85percent) of 1-(tert-butoxycarbonyl)-2,3,6,7-tetrahydro-5-methoxy-(1H)-1,4-diazepine as a yellow liquid. 1 H NMR(400 MHz, CD3 OD): delta3.58 (s, 3H), 3.53-3.45 (m, 6H), 2.63-2.59 (m, 2H), 1.46 (s, 9H). Mass spectrum: m/z=129.
100 mg In dichloromethane; at 0 - 20℃; 6.01.22.05 5-Methoxy-2,3,6,7-tetrahydro-(1,4)-diazepine-1-carboxylic acid tert-butyl ester 77.5 mg trimethyloxonium tetrafluoroborate was added to 100 mg <strong>[190900-21-1]5-oxo-[1,4]diazepane-1-carboxylic acid tert-butyl ester</strong> in 2 mL dichlormethane at 0-5° C. The reaction mixture was stirred over night at RT. The reaction was washed with saturated sodium hydrogencarbonate solution and water and evaporated to yield 100 mg of the desired product. Rt: 0.79 min (method B), (M+H)+: 229
100 mg In dichloromethane; at 0 - 20℃; 5-Methoxy-2, 3, 6, 7-tetrahydro-(l, 4)-diazepine-l-carboxylic acid tert-butyl ester 77.5 mg trimethyloxonium tetrafluoroborate was added to 100 mg 5-oxo-[l, 4] diazepane-1- carboxylic acid tert-butyl ester in 2 mL dichlormethane at 0-5 °C. The reaction mixture was stirred over night at RT. The reaction was washed with saturated sodium hydro gencarbonate solution and water and evaporated to yield 100 mg of the desired product. Rt: 0.79 min (method B), (M+H) : 229
  • 2
  • trimethyl oxonium tetrafluoroborate [ No CAS ]
  • [ 190900-21-1 ]
  • [ 190900-22-2 ]
YieldReaction ConditionsOperation in experiment
In dichloromethane; at 20℃; To a solution of tert-butyl 5-oxo-1,4-diazaperhydroepin carboxylate in dichloromethane (400 mL), trimethyl tetrafluoroborate oxonium (33.86 g) was added and stirred overnight at room temperature. To the reaction mixture were added an aqueous solution of saturated sodium bicarbonate (200 mL) and water (100 mL), and then after stirring for 20 minutes, the aqueous layer was removed and the organic layer was dried on anhydrous magnesium sulfate, and filtered. The solvent was evaporated under reduced pressure, and the residue dried under vacuum to obtain a crude title compound as a oily compound. The product thus obtained was used in the subsequent reaction without further purification.
 

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