Home Cart Sign in  
Chemical Structure| 1225276-07-2 Chemical Structure| 1225276-07-2

Structure of 1225276-07-2

Chemical Structure| 1225276-07-2

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

4.5 *For Research Use Only !

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

US Stock

Global Stock

In Stock
{[ item.pr_size ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

  • {[ item.pr_size ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of [ 1225276-07-2 ]

CAS No. :1225276-07-2
Formula : C13H22BrNO2
M.W : 304.22
SMILES Code : O=C(N(CC1)CCC21CC(Br)C2)OC(C)(C)C
MDL No. :MFCD24471158
InChI Key :GACABBWTCSUAEK-UHFFFAOYSA-N
Pubchem ID :67371301

Safety of [ 1225276-07-2 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 1225276-07-2 ]

* 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 [ 1225276-07-2 ]

[ 1225276-07-2 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 1225276-07-2 ]
  • [ 871125-82-5 ]
  • [ 1225276-52-7 ]
YieldReaction ConditionsOperation in experiment
With nickel(II) iodide; trans-2-aminocyclohexan-1-ol; sodium hexamethyldisilazane; In isopropyl alcohol; at 70℃;Inert atmosphere; Example 40; Synthesis of N-(3,4-dimethylisoxazol-5-yl)-2-{4-[(4-fluorobenzyl)oxy]phenyl}-7-azaspiro[3.5]nonane-7-carboxamide A 0.4 M stock solution of 2-bromo-7-aza-spiro[3.5]nonane-7-carboxylic acid tert-butyl ester in anhydrous isopropanol (0.5 mL, 0.200 mmol) and a 0.024 M stock solution of trans 2-aminocyclohexanol in isopropanol (0.5 mL, 0.012 mmol, 0.06 equiv) was added to a vial containing sodium hexamethyldisilazide (0.400 mmol, 2 equiv), nickel iodide (0.012 mmol, 0.06 equiv), and <strong>[871125-82-5]{4-[(4-fluorobenzyl)oxy]phenyl}boronic acid</strong> (0.400 mmol, 2 equiv; CAS No.871125-82-5). The vial was flushed with nitrogen, capped, and shook at 70 C. overnight. The reaction mixtures were concentrated under vacuum to give the crude tert-butyl carbamate derivative. The residue was dissolved in dichloromethane (1.2 mL) and treated with 4 N HCl in dioxane (0.8 mL). After shaking for 2 h, the reaction mixture was concentrated under vacuum to give the crude amine hydrochloride salt derivative. The crude amine hydrochloride salt residue was dissolved in acetonitrile (2.0 mL) and split into two separate vials (1.0 mL, 0.1 mmol each). To the solution in one of the vials was added diisopropylethylamine (0.17 mL, 1.0 mmol, 10 equiv) followed by a solution of phenyl(3,4-dimethylisoxazol-5-yl)carbamate (0.120 mmol in acetonitrile, 1.2 equiv). After shaking overnight at rt, the reaction was concentrated under vacuum, diluted in DMSO (1.5 mL), filtered through celite, and purified by reverse phase HPLC (acetonitrile/water/0.05% trifluoroacetic acid) to give the title compound (8.5 mg). LCMS (Phenomenex Gemini C18 4.6×50 mm 5 mum (0.04% Formic Acid, 0.01% TFA/MeCN)) tR 2.23 min; m/z 464.45 (MH+).
  • 2
  • [ 1225276-07-2 ]
  • [ 35344-95-7 ]
  • tert-butyl 2-(4-formyl-1H-pyrazol-1-yl)-7-azaspiro[3.5]nonane-7-carboxylate [ No CAS ]
YieldReaction ConditionsOperation in experiment
With caesium carbonate;Inert atmosphere; In this case, C3 was reacted with <strong>[35344-95-7]1H-<strong>[35344-95-7]pyrazole-4-carbaldehyde</strong></strong> and cesium carbonate to afford tert-butyl 2-(4-formyl-1H-pyrazol-1-yl)-7-azaspiro[3.5]nonane-7-carboxylate. This material was treated with (diethylamino)sulfur trifluoride to provide the requisite tert-butyl 2-[4-(difluoromethyl)-1H-pyrazol-1-yl]-7-azaspiro[3.5]nonane-7-carboxylate.
 

Historical Records

Technical Information

Categories