HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tert-Butylamine → HCID 23335502, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tert-Butylamine | HCID 6385 | — |
| Reactant | HCID 23335530 | HCID 23335530 | — |
| Product | HCID 23335502 | HCID 23335502 | 55% |
Reaction Steps
1.5 g of 4-(2,3-epoxypropoxy)-2-carbamoyl-6-methyl indole in 25 ml tert.-butylamine is heated to boiling for 24 hours. The solution is then evaporated and the residue dissolved in chloroform. The chloroform solution is washed with water, dried and evaporated. The residue is suspended in hot acetic ester and mixed with 0.8 g benzoic acid. A clear solution will result here, from which a precipitate deposits. This is aspirated and recrystallized from 100 ml acetic ester. There is obtained 1.5 g (55% of theory) 4-(2-hydroxy-3-tert.-butylaminopropoxy)-2-carbamoyl-6-methyl indole as benzoate; m.p. 213°-214° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04229464 |
| Source dataset | uspto-grants-1980_10 |
| ORD ID | ord-d5b4616308f64dc4a93e5e2d5e6b4f82 |
| Source note | uspto-grants-1980_10 |