HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → HCID 131719702, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Oxalic Acid | HCID 971 | — |
| Reactant | (2s)-Glycidyl indol-4-yl ether | HCID 10943254 | — |
| Reactant | 4-(Naphthalen-2-yl)piperidine | HCID 22029264 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 131719702 | HCID 131719702 | — |
Reaction Steps
The title compound was prepared in similar fashion from (S)-(+)-4-(oxiranylmethoxy)-1H-indole and 4-(2-naphthyl)piperidine. The resulting free base was dissolved in ethyl acetate, and precipitated with one equivalent of oxalic acid in ethyl acetate in 74% overall yield. mp. 171°-172°. FDMS m/e=400 (M+ of free base). α[D]589 =-13.51 (c=1.04, methanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05614523 |
| Source dataset | uspto-grants-1997_03 |
| ORD ID | ord-361976b23d854519b88a782e165526ba |
| Source note | uspto-grants-1997_03 |