Synthesis method of nitrogen-(benzoxycarbonyl piperidine-4-yl)-2-(trifluoromethyl)benzamide
A technology of benzyloxycarbonylpiperidine and trifluoromethyl, which is applied in the field of practical synthesis of nitrogen-2-benzamide, can solve the problems of no industrialized synthetic route report, and achieve the purpose of filling the blank of industrialized synthesis and reaction Reasonable process design to avoid the effect of post-processing
Patent Information
- Authority / Receiving Office
- CN · China
- Patent Type
- Applications(China)
- Current Assignee / Owner
- Publication Date
- 2019-03-22
- Estimated Expiration
- Not applicable · inactive patent
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Figure 1
Abstract
Description
technical field
[0001] The invention relates to a practical synthesis method of nitrogen-(benzyloxycarbonylpiperidin-4-yl)-2-(trifluoromethyl)benzamide. Background technique
[0002] Nitrogen-(benzyloxycarbonylpiperidin-4-yl)-2-(trifluoromethyl)benzamide, CAS No. 7732-18-5, currently has no industrialized synthetic route report. Contents of the invention
[0003] The purpose of this invention is to develop a kind of simple, general nitrogen-(benzyloxycarbonyl piperidin-4-yl)-2-(trifluoromethyl) benzamide synthetic method, mainly solve the technology that does not have industrialized synthetic route at present question.
[0004] Technical scheme of the present invention: a kind of synthetic method of nitrogen-(benzyloxycarbonylpiperidin-4-yl)-2-(trifluoromethyl)benzamide, nitrogen-(piperidin-4-yl)-2 -(trifluoromethyl)benzamide and sodium carbonate were added to tetrahydrofuran and water, benzyl chloroformate was slowly added dropwise, and the reaction was post-treated to ...
Examples
Embodiment 1
[0009] Synthesis of Nitrogen-(Benzyloxycarbonylpiperidin-4-yl)-2-(trifluoromethyl)benzamide
[0010]
[0011] 3 grams of compound 1 and 4.7 grams of sodium carbonate were added to a mixed solvent of 25 mL of tetrahydrofuran and 25 mL of water, the mixture was cooled to 0 degrees Celsius, and 2 grams of compound 2 was slowly added dropwise to the above suspension under stirring, controlled Throughout the dropping process, the temperature was kept at 0°C. After the dropwise addition was completed, the reaction was carried out at 0° C. for 2 hours.
[0012] After the reaction was completed, the reaction liquid was extracted twice with 50 mL of dichloromethane, the organic phase was collected, washed once with 50 mL of saturated brine, the organic phase was dried with sodium sulfate, filtered and spin-dried to obtain the crude compound 3, and the crude compound 3 was obtained using 30 mL of methyl The tert-butyl ether was beaten, and the solid was collected to obtain 3.4 g of ...