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HRID 1900921作成日:2026年10月23日

Methanol → (2S)-(-)-1-(4-indolyloxy)-3-(4-(2,6-dimethylphenyl)piperazin-1-yl)-2-propanol ethanedioate

https://huagongshe.com/ja/reaction/1900921

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物Oxalic AcidHCID 971—
反応物1-(2,6-Xylyl)piperazineHCID 70538—
反応物(2s)-Glycidyl indol-4-yl etherHCID 10943254—
溶媒Ethyl AcetateHCID 8857—
生成物(2S)-(-)-1-(4-indolyloxy)-3-(4-(2,6-dimethylphenyl)piperazin-1-yl)-2-propanol ethanedioateHCID 131719666—

反応手順

The title compound was prepared in similar fashion from (S)-(+)-4-(oxiranylmethoxy)-1H-indole and 1-(2,6-dimethylphenyl)piperazine. The resulting free base was dissolved in ethyl acetate, and precipitated with one equivalent of oxalic acid in ethyl acetate in 50% overall yield. FDMS m/e=379 (M+ of free base). α[D]589 =-11.89 (c=0.47, methanol).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05576321
出典データセットuspto-grants-1996_11
ORD IDord-83d25df6270941f895956729f636ed19
出典メモuspto-grants-1996_11