HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 56989982, compound → HCID 86742269, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 56989982 | HCID 56989982 | — |
| Reactant | HCID 86742270 | HCID 86742270 | — |
| Product | HCID 86742269 | HCID 86742269 | — |
Reaction Steps
A solution of 5-n-butyloctahydro-2-oxo-1H-indoleacetic acid ethyl ester (3aα, 7aα) (VI) (5.0 g, 0.0178 mole) in N,N-bis-(1-methylethyl)aminoethylamine (4.49 g, 0.0267 mole) is heated at 100° C. for 18 hours. The solution is concentrated at reduced pressure to an oil. The oil is dissolved in 2-propanol and the solution is treated with a saturated solution of hydrogen chloride in 2-propanol. The solution is diluted with anhydrous diethyl ether and allowed to crystallize. The crystals are filtered. Recrystalliztion from acetonitrile-diethyl ether yields pure 5-n-butyloctahydro-2-oxo-1H-indoleacetamide N-[bis[1-methylethyl]amino]ethyl]·hydrochloride (3aα, 7aα) (VII) with mp 116°-118° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04758585 |
| Source dataset | uspto-grants-1988_07 |
| ORD ID | ord-cd973947d5ae494c95e5dd2aa2a51a8c |
| Source note | uspto-grants-1988_07 |