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HRID 481602作成日:2026年10月25日

Methanol → (2s)-(-)-1-(4-Indolyloxy)-3-(4-phenoxypiperidin-1-yl)-2-propanol ethanedioate

https://huagongshe.com/reaction/481602

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4-PhenoxypiperidineHCID 18878—
反応物(2s)-Glycidyl indol-4-yl etherHCID 10943254—
溶媒Ethyl AcetateHCID 8857—
生成物(2s)-(-)-1-(4-Indolyloxy)-3-(4-phenoxypiperidin-1-yl)-2-propanol ethanedioateHCID 131719687—

反応手順

The title compound was prepared in similar fashion from (S)-(+)-4-(oxiranylmethoxy)-1H-indole and 4-(phenoxy)piperidine. The resulting free base was dissolved in ethyl acetate, and precipitated with one equivalent of oxalic acid in ethyl acetate in 69% overall yield. FDMS m/e=366 (M+ of free base). α[D]589 =-14.29 (c=0.5, 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-6e934172234940b59a65106d36e98ad6
出典メモuspto-grants-1998_08