HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 19773377, compound → HCID 19773412, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 19773377 | HCID 19773377 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19773412 | HCID 19773412 | — |
Reaction Steps
Starting from 0.56 g (1.89 mmol) of 5-(N-acetyl-N-methyl-amino)-2-n-propylamino-tetraline-hydrochloride (Example 4.7.8) which is converted into the base, the title compound is obtained as a base by reduction in 20 ml of absolute tetrahydrofuran analogously to Example 4.5.1 c), but using 1.90 ml of 2-molar diboran solution in tetrahydrofuran (THF) as reducing agent. The base is purified by column chromatography (50 g of silica gel, methylene chloride/methanol/conc. ammonia 90:10:0.5) and crystallised as the dihydrochloride analogously to Example 4.1.1, in a yield of 0.33 g (54.6% of theory) and with a melting point of 200° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05196454 |
| Source dataset | uspto-grants-1993_03 |
| ORD ID | ord-cc6214b6ad4b446cbc09afdf19b29a49 |
| Source note | uspto-grants-1993_03 |