HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tert-Butylamine → 4-(2-Hydroxy-3-tert.-butylamino-propoxy)-2-ethoxycarbonyl-6-methylindole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tert-Butylamine | HCID 6385 | — |
| Reactant | 4-(2,3-Epoxypropoxy)-2-ethoxycarbonyl-6-methyl indole | HCID 20527529 | — |
| Product | 4-(2-Hydroxy-3-tert.-butylamino-propoxy)-2-ethoxycarbonyl-6-methylindole | HCID 23335543 | 71% |
Reaction Steps
1.7 g 4-(2,3-epoxypropoxy)-2-ethoxycarbonyl-6-methyl-indole are dissolved in 25 ml tert.-butylamine. The solution is stored at room temperature for three days and then evaporated in vacuum. The residue is triturated with ether and aspirated. The crude product is dissolved in hot acetic ester and the solution is mixed with 0.3 ml glacial acetic acid. The precipitate resulting after cooling of the solution is aspirated and dried. There is obtained 1.8 g (~71% of theory) of 4-(2-hydroxy-3-tert.-butylamino-propoxy)-2-ethoxycarbonyl-6-methylindole as acetate; m.p. 181°-183° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04229464 |
| Source dataset | uspto-grants-1980_10 |
| ORD ID | ord-19836387e9c64fbdbc345a28c56ffee8 |
| Source note | uspto-grants-1980_10 |