Examples of 'desired amine' in a sentence
Meaning of "desired amine"
desired amine: a chemical compound or substance, typically referring to an organic compound containing an amino group, that is sought after or required for a specific purpose
How to use "desired amine" in a sentence
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desired amine
The desired amine was purified using column chromatography.
Catalytic hydrogenation then yields the desired amine.
The desired amine is thus isolated without further purification.
Evaporation of the solvent afforded the crude desired amine.
The desired amine can be realized vía transformations previously discussed.
Concentration under reduced pressure gives the desired amine.
This afforded the desired amine as a white solid in quantitative yield.
Deprotection as described above gives the desired amine IIIc.
HPLC to give the desired amine as a colourless oil.
The organic extracts were concentrated giving the desired amine.
Standard aqueous workup gave the desired amine as a pale yellow oil.
The reaction is filtered and evaporated to yield the desired amine.
A stock solution in DMF of the desired amine is prepared in a desired container.
This amide may then be reduced to afford the desired amine.
The desired amine was liberated by treatment of aq . ammonia during extraction into chloroform.
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The solvent was evaporated to give the desired amine as a white solid.
Other 2-carboxamide derivatives were prepared in a similar fashion by replacing ammonia with the desired amine.
The phthalimide is then converted to the desired amine by reaction with hydrazine.
The catalyst was filtered and the solvent was evaporated to give the desired amine.
After concentration to dryness, 124 g of the desired amine is recovered as a viscous oil.
The methansulfonyloxy ( mesyl ) leaving group can then be replaced by the desired amine.
Treatment of this carbamate with the desired amine 6 provides the urea 7.
The separated imine product from step ( b ) is then hydrogenated to form the desired amine.
The desired amine 28 is then furnished by coupling the pyridine acid 8 with aniline 27.
These halo analogues were chosen as ideal precursors to the desired amine products.
The desired amine was added to the reaction at -78 °C under an inert atmosphere.
The reduction takes place with high stereoselectivity to give the desired amine isomer.
Simple SnAr substitution with the desired amine ( R1NH ) can afford substituted pyrimidines ( 1d ).
The Formula LXII compound is deprotected to afford the desired amine intermediate.
The process of the present invention preferably yields at least 50 percent of the desired amine.
The removal of the protecting group affords the desired amine of formula IX.
Afterward, silica gel column chromatography was done to obtain 2.6 g of the desired amine.
The aldehyde 27 is then reductively aminated with the desired amine to afford the compound 28.
Removal of the N-benzyl protecting group gives the desired amine.
Purification by HPLC followed by freeze-drying produced the desired amine as a TFA salt.
Treatment with 5N hydrochloric acid removes the protecting benzoyl group to give the desired amine product.
An acid, such as HCl, is added dropwise to a desired amine in water.
Reduction of compound 24 with cobalt chloride and sodium borohydride provides the desired amine 25.
The chloride 50 is then displaced with an amine source to afford the desired amine component 51.
Evaporation of the solvents under reduced pressure provided 4.63 g of the desired amine mass spec.
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Examples of using Desired
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Turn until the desired volume is gained
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