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HRID 323828作成日:2026年10月25日

Acetone → N-[4-(2-methyl-2H-tetrazol-5-yl)phenylmethyl]-4-[bis(4-trifluoromethoxyphenyl)hydroxymethyl]piperidine

https://huagongshe.com/reaction/323828

反応式

関与物質

役割名称HCID仕込み量
反応物AcetoneHCID 180—
反応物DiisopropylethylamineHCID 81531—
反応物5-(4-Bromomethylphenyl)-2-methyl-2H-tetrazoleHCID 589329—
反応物4-[Bis(4-trifluoromethoxyphenyl)hydroxymethyl]piperidineHCID 19040926—
溶媒Dimethyl SulfoxideHCID 679—
溶媒DichloromethaneHCID 6344—
生成物N-[4-(2-methyl-2H-tetrazol-5-yl)phenylmethyl]-4-[bis(4-trifluoromethoxyphenyl)hydroxymethyl]piperidineHCID 1551518532.9%

反応手順

This compound was prepared in a manner analogous to that of Step D of Example 4, with 0.3 gram (0.001 mole) of 4-(2-methyl-2H-tetrazol-5-yl)phenylmethyl bromide, 0.5 gram (0.001 mole) of 4-[bis(4-trifluoromethoxyphenyl)hydroxymethyl]piperidine (prepared as in Step C of Example 4), and 0.6 gram (0.004 mole) of N, N-diisopropylethylamine in about 5 mL of dimethyl sulfoxide as reagents. The crude reaction product was subjected to column chromatography on silica gel, with 3:7 acetone:methylene chloride as the eluant. The product-containing fractions were combined and concentrated under reduced pressure, yielding about 0.2 gram of N-[4-(2-methyl-2H-tetrazol-5-yl)phenylmethyl]-4-[bis(4-trifluoromethoxyphenyl)hydroxymethyl]piperidine. The NMR spectrum was consistent with the proposed structure.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06214845B1
出典データセットuspto-grants-2001_04
ORD IDord-fc577bffcbe54cceb0a10f05dbad7bd6
出典メモuspto-grants-2001_04