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[ CAS No. 1462921-50-1 ] {[proInfo.proName]}

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Chemical Structure| 1462921-50-1
Chemical Structure| 1462921-50-1
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Product Details of [ 1462921-50-1 ]

CAS No. :1462921-50-1 MDL No. :MFCD23703584
Formula : C5H11ClN2O Boiling Point : -
Linear Structure Formula :- InChI Key :XQJHPSIERFKZFW-UHFFFAOYSA-N
M.W : 150.61 Pubchem ID :84819331
Synonyms :

Safety of [ 1462921-50-1 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 1462921-50-1 ]

* 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 [ 1462921-50-1 ]

[ 1462921-50-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 75-36-5 ]
  • [ 91188-13-5 ]
  • [ 1462921-50-1 ]
YieldReaction ConditionsOperation in experiment
550 mg A solution of tert-butyl azetidin-3-ylcarbamate (1.00 g, 5.81 mmol) [Ark Pharma, AK26432] in tetrahydrofuran (50 mL) was treated with triethylamine (1.6 mL, 11.6 mmol) followed by N,N-dimethylformamide (15 mL) and cooled to 0 C. The reaction mixture was treated with acetyl chloride (495 muL, 6.97 mmol) and stirred overnight at room temperature. The reaction mixture was diluted with ether and washed with water and brine, dried over magnesium sulfate, filtered, and concentrated give a crude residue that was used immediately without purification. The intermediate azetidine was diluted with methylene chloride (30 mL), treated with 4.0 M hydrogen chloride in dioxane (22.0 mL, 88.0 mmol), and stirred at rt for 30 min. The reaction mixture was diluted with ether and the precipitated solid was collected by filtration in order to give the desired product (550 mg, 63%) as a HCl salt. LCMS calculated for C5H11N20 (M+H)+: m/z=115.1. found: 115.2.
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