- Method for preparing 2, 3-dihydro-2-oxo-1H-benzimidazole-1-butyric acid
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The invention relates to a method for preparing 2, 3-dihydro-2-oxo-1H-benzimidazole-1-butyric acid, which comprises the following steps of: dehydrating 1, 3-dihydro-1-(1-methylvinyl)-2H-benzimidazole-2-one in an organic solvent at 100-120 DEG C under the action of an acid-binding agent, adding ethyl 4-bromobutyrate for reaction after dehydration, cooling the reaction liquid to 70-90 DEG C after the reaction is finished, adding water preheated to 40-60 DEG C, stirring and splitting phases at proper time; and adding alkali into an organic phase, carrying out saponification reaction under the environment of 45-80 DEG C and 150-200 mbar, slowly adding hydrochloric acid at the temperature of 40-60 DEG C after the saponification reaction is finished, then reacting for 2-4 hours at the temperature of 90-110 DEG C, cooling, filtering, washing a filter cake with water, and drying the filter cake to constant weight at 50-70 DEG C and 100-180 mbar. Potassium carbonate is used to replace sodium hydride, so that the problems of high potential safety hazard, serious three-waste pollution and the like in the traditional process are fundamentally eliminated, the production process is simpler and more convenient by frying in one pot, and the production cost is reduced; and meanwhile, the method is simple, convenient and safe to operate, reasonable in process condition, high in reaction yield and relatively high in implementation value.
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- PROCESS FOR MAKING A CRYSTALLINE ZILPATEROL SALT
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This invention generally relates to processes for making a crystalline zilpaterol salt, particularly zilpaterol hydrochloride. This invention also relates to methods of treatment using a crystalline zilpaterol salt prepared in accordance with this invention to increase the rate of weight gain, improve feed efficiency, and/or increase carcass leanness in livestock, poultry, and fish.
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Page/Page column 13
(2012/03/26)
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- PROCESS FOR MAKING A CRYSTALLINE ZILPATEROL SALT
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This invention generally relates to processes for making a crystalline zilpaterol salt, particularly zilpaterol hydrochloride. This invention also relates to methods of treatment using a crystalline zilpaterol salt prepared in accordance with this invention to increase the rate of weight gain, improve feed efficiency, and/or increase carcass leanness in livestock, poultry, and fish.
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Page/Page column 20; 21
(2010/08/05)
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- HETEROCYCLIC COMPOUNDS USEFUL AS ANABOLIC AGENTS FOR LIVESTOCK ANIMALS
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Compounds of formula (I) and pharmaceutically acceptable salts thereof are agonists at the beta-2 adrenoceptor. They are useful as feed additives for livestock animals.
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- BENZAZEPIN-2(1H)-ONE DERIVATIVES
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Compounds of formula (I) and pharmaceutically acceptable salts thereof are agonists at the beta-2 adrenoceptor. They are useful as feed additives for livestock animals.
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Page/Page column 7; 42
(2008/06/13)
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- PROCESSES FOR MAKING ZILPATEROL AND SALTS THEREOF
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This invention generally relates to processes for making zilpaterol and salts thereof, as well as processes for making intermediates that, inter alia, may be used to make zilpaterol and salts thereof. The zilpaterol and salts prepared in accordance with this invention can be used to increase the rate of weight gain, improve feed efficiency, and/or increase carcass leanness in livestock, poultry, and fish.
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Page/Page column 12; 30; 31; 38; 40-41
(2008/12/04)
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- Synthesis of imidazobenzazepinthiones: A new series of HIV-1 reverse transcriptase inhibitors
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A general route to a series of novel imidazobenzazepines that are 'carba' analogs of the TIBO class of non-nucleoside HIV-1 reverse transcriptase inhibitors has been developed. A pair of allyl side-chain containing compounds were found to have significant HIV-1 inhibitory activity.
- Salaski, Edward J.
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p. 1387 - 1390
(2007/10/02)
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