133863-87-3Relevant articles and documents
A practical synthesis of 2-methoxy-6-trifluoromethylaniline
Pews, R. Garth
, p. 65 - 67 (1998)
A practical synthesis of 2-methoxy-6-trifluoromethylaniline is described via halogenation, nitration and reduction of 3-trifluoromethylanisole.
Preparation method of trifluoromethylamine
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Paragraph 0023-0026; 0027-0045; 0046-0056; 0076-0086, (2018/09/28)
The invention relates to a preparation method of trifluoromethylamine. The method includes the following steps that aromatic amine shown in the formula (1) and a trifluoromethyl reagent shown in the formula (2) react in a solvent under the condition that an alkali and/or nickel compound exists, and the trifluoromethylamine compound shown in the formula (3) is generated. According to the preparation method of trifluoromethylamine, aromatic amine and 1-trifluoromethyl-1,2-iodobenzoyl-3(H)-ketone serve as raw materials and react under the condition that the alkali and/or nickel compound exists through the amino positioning effect on aromatic nucleus. The synthesis steps of the method are simple, the cost of the raw materials is low, the production cost of trifluoromethylamine can be greatly reduced, and large-scale industrialized production is promoted.
THERAPEUTIC ARYL-AM I DO-ARYL COMPOUNDS AND THEIR USE
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Page/Page column 171-172, (2011/04/14)
The present invention pertains generally to the field of therapeutic compounds, and more specifically to certain aryl-amido-aryl compounds of the following formula (for convenience, collectively referred to herein as "AAA compounds"), which, inter alia, a