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[ CAS No. 53929-74-1 ] {[proInfo.proName]}

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Chemical Structure| 53929-74-1
Chemical Structure| 53929-74-1
Structure of 53929-74-1 * Storage: {[proInfo.prStorage]}
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Product Details of [ 53929-74-1 ]

CAS No. :53929-74-1 MDL No. :MFCD09833117
Formula : C5H12BrN Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 166.06 Pubchem ID :-
Synonyms :

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Application In Synthesis of [ 53929-74-1 ]

* 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 [ 53929-74-1 ]

[ 53929-74-1 ] Synthesis Path-Downstream   1~7

  • 1
  • [ 3306-69-2 ]
  • [ 53929-74-1 ]
  • [ 105208-63-7 ]
YieldReaction ConditionsOperation in experiment
With sodium amide; toluene
  • 2
  • [ 14733-68-7 ]
  • [ 53929-74-1 ]
  • [ 19420-42-9 ]
YieldReaction ConditionsOperation in experiment
With potassium hydroxide In 2-ethoxy-ethanol for 6h;
  • 3
  • [ 53929-74-1 ]
  • [ 6972-05-0 ]
  • [ 95930-56-6 ]
YieldReaction ConditionsOperation in experiment
80% With hydrogen bromide In isopropyl alcohol for 2h; Heating;
  • 4
  • [ 53929-74-1 ]
  • [ 78286-57-4 ]
  • [ 95930-60-2 ]
YieldReaction ConditionsOperation in experiment
90% With hydrogen bromide In isopropyl alcohol for 2h; Heating;
  • 6
  • [ 55453-87-7 ]
  • [ 53929-74-1 ]
  • [ 113806-05-6 ]
YieldReaction ConditionsOperation in experiment
81.2% Lithium naphthalene reagent preparation Lithium metal (0.4 g, 60 mmol) was added to anhydrous naphthalene (2.6 g, 20 mmol) under nitrogen protection In the temperature control 20-25 ° C stirring 2h lithium naphthalene reagent.Preparation of highly active organozinc reagent Under nitrogen protection, 3-bromo-N,N-dimethylpropanamine (5.0 g, 30 mmol) was added to the reaction flask, anhydrous tetrahydrofuran (32 ml), and the mixture was stirred and cooled to 10-20 °C. Zinc bromide (13.5 g, 60 mmol) was added in batches, stirred for 10 minutes, and the above-mentioned naphthalene lithium reagent was added dropwise. After the reaction temperature was stabilized, the mixture was heated to reflux (65-70° C.), and the reaction was stirred for 5-6 h. The resulting reaction solution is a highly active organozinc reagent.Preparation of Crude Olopatadine <strong>[55453-87-7]Isoxepac</strong>(4.0g, 15mmol) was dissolved in tetrahydrofuran (12ml), dissolved and clarified, and the temperature was controlled at 0-10°C.In the above high activity organozinc reagent, after about 0.5 h, the reaction mixture was heated to 20-25° C. and stirred for 16 h. The end point of the reaction was followed by HPLC, and the purity was 94.0percent. The reaction solution was cooled, and 25 ml of water was added for extraction. The pH of the aqueous phase was adjusted to pH 4.0 to 4.4. The aqueous phase was washed with n-hexane, methyl tert-butyl ether, and ethyl acetate, respectively, and n-butanol was extracted with 20 ml×4 of water to decolorize. Evaporated under reduced pressure to give 4.4 g of oil, with a purity of 96.0percent.Refined OlrotidineTo the above-obtained oily substance, n-butanol (20 ml) was added, heated to 75-80°C, and stirred for 15 minutes.But to 5-10 ° C, stirring crystallized 1h, filtered and dried to give 3.6g olopatadine, yield 81.2percent, purity 99.2percent.
  • 7
  • [ 32943-25-2 ]
  • [ 53929-74-1 ]
  • [ 303-49-1 ]
YieldReaction ConditionsOperation in experiment
66% Stage #1: 3-chloro-10,11-dihydro-5H-dibenzo[b,f]azepine With sodium hydride In tetrahydrofuran at 110℃; for 2h; Glovebox; Inert atmosphere; Schlenk technique; Stage #2: N,N-dimethyl-3-bromopropylamine In tetrahydrofuran at 110℃; for 22h; Glovebox; Inert atmosphere; Schlenk technique;
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