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- W2606142214 abstract "3-Methylaminocamphor and 3-ethylaminocamphor were obtained in a good yield from 3-formamidocamphor. Application of haloacyl halides to 3-methyl- and 3-ethyl-aminocamphor afforded (N-methyl(or ethyl)-2-haloacylamino)camphors (VI to XIV) and these were converted to 3-[N-alkyl-2-dialkyl(allyl)amino(piperidyl)acylamino]-camphors (XV to XL) by condensation with dialkyl(allyl)amine and piperidine. The same reactions were carried out with 3-camphorylurea and 1-(2-haloacyl)-3-(3-camphoryl)ureas (XLI to XLIII), and 1-(2-dimethyl(or ethyl)aminoacyl)-3-(3-camphoryl)ureas (XLIV to XLIX) were obtained. 1-(2-Dialkylaminoacyl)-3-(3-camphoryl)-3-methyl(or ethyl)ureas were not isolated in crystalline form." @default.
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- W2606142214 date "1959-01-01" @default.
- W2606142214 modified "2023-10-17" @default.
- W2606142214 title "Syntheses of Analgesics. XX" @default.
- W2606142214 doi "https://doi.org/10.1248/yakushi1947.79.2_162" @default.
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