HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → (2S)-(-)-1-(4-indolyloxy)-3-(4-(2-trifluoromethylphenyl)piperazin-1-yl)-2-propanol ethanedioate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Oxalic Acid | HCID 971 | — |
| Reactant | 1-[2-(Trifluoromethyl)phenyl]piperazine | HCID 2777670 | — |
| Reactant | (2s)-Glycidyl indol-4-yl ether | HCID 10943254 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (2S)-(-)-1-(4-indolyloxy)-3-(4-(2-trifluoromethylphenyl)piperazin-1-yl)-2-propanol ethanedioate | HCID 131719672 | — |
Reaction Steps
The title compound was prepared in similar fashion from (S)-(+)-4-(oxiranylmethoxy)-1H-indole and 1-(2-trifluoromethylphenyl)piperazine. The resulting free base was dissolved in ethyl acetate, and precipitated with one equivalent of oxalic acid in ethyl acetate in 70% overall yield. mp 123°-124°. FDMS m/e=419 (M+ of free base). α[D]589 =-7.01(c=0.66, methanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05741789 |
| Source dataset | uspto-grants-1998_04 |
| ORD ID | ord-7bb3038bfb9d4b50a6d73b2260a187ac |
| Source note | uspto-grants-1998_04 |