HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → (2S)-(-)-1-(4-indolyloxy)-3-(4-bis(4-chlorophenyl)methylpiperazin-1-yl)-2-propanol ethanedioate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Oxalic Acid | HCID 971 | — |
| Reactant | 1-[Bis(4-chlorophenyl)methyl]piperazine | HCID 285510 | — |
| Reactant | (2s)-Glycidyl indol-4-yl ether | HCID 10943254 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (2S)-(-)-1-(4-indolyloxy)-3-(4-bis(4-chlorophenyl)methylpiperazin-1-yl)-2-propanol ethanedioate | HCID 131719670 | — |
Reaction Steps
The title compound was prepared in similar fashion from (S)-(+)-4(oxiranylmethoxy)-1H-indole and 1-(bis(4-chlorophenyl)methylpiperazine. The resulting free base was dissolved in ethyl acetate, and precipitated with one equivalent of oxalic acid in ethyl acetate in 82% overall yield. mp 123-124°. FDMS m/e=510 (M+ of free base). α[D]589=−8.46 (c=0.89, methanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06172073B2 |
| Source dataset | uspto-grants-2001_01 |
| ORD ID | ord-b1807a88e8984a38a782a39c4b7d798b |
| Source note | uspto-grants-2001_01 |