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HRID 481581作成日:2026年10月27日

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

https://huagongshe.com/reaction/481581

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US05789402
出典データセットuspto-grants-1998_08
ORD IDord-0b5cbbbaf1b9430a9e2e28afd09b826c
出典メモuspto-grants-1998_08