HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → (1-n Butyl-4-piperidyl)methyl-2,3-dihydrothiazolo[3,2-a]indole-9-Carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 2,3-Dihydrothiazolo[3,2-a]indole-9-carboxylic acid | HCID 19599448 | — |
| Product | (1-n Butyl-4-piperidyl)methyl-2,3-dihydrothiazolo[3,2-a]indole-9-Carboxylate | HCID 86753467 | 31% |
Reaction Steps
The title compound was prepared from 2,3-dihydrothiazolo[3,2-a]indole-9carboxylic acid (D15) using the method of Example 10. The crude product was purified by chromatography on silica gel eluting with 5% methanol/chloroform to give a yellow oil. This was passed through a plug of basic alumina eluting with ethyl acetate to afford the title compound as a pale yellow oil (31%) which was converted to its oxalate salt and was crystallised from acetone as an off-white solid mp 212°-215° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05852014 |
| Source dataset | uspto-grants-1998_12 |
| ORD ID | ord-a16819e780df4aa4a96d9770e9e4cc7e |
| Source note | uspto-grants-1998_12 |