HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isopropanol hydrochloride → (R)-2-Fluoro-5,11-dihydro-5-[1-(4-pyrrolidinophenethyl)pyrrolidin-2-yl-methyl]dibenzo[b,e][1,4]oxazepine dihydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isopropanol hydrochloride | HCID 21912024 | — |
| Reactant | (R)-2-fluoro-5,11-dihydro-5-[1-(4-pyrrolidinophenethyl)pyrrolidin-2-ylmethyl]dibenzo[b,e][1,4]oxazepine | HCID 59644017 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | (R)-2-Fluoro-5,11-dihydro-5-[1-(4-pyrrolidinophenethyl)pyrrolidin-2-yl-methyl]dibenzo[b,e][1,4]oxazepine dihydrochloride | HCID 69199662 | — |
Reaction Steps
(R)-2-Fluoro-5,11-dihydro-5-[1-(4-pyrrolidinophenethyl)pyrrolidin-2-ylmethyl]dibenzo[b,e][1,4]oxazepine (12.04 g, 25.5 mmol) was dissolved in 2-propanol (250 ml). 4 M hydrogen chloride/2-propanol (17.0 ml) was added to the obtained solution and they were stirred at room temperature for 0.5 hour. The solvent was evaporated under reduced pressure, and 2-propanol (about 50 ml) was added to the residue. The solvent was evaporated under reduced pressure repeatedly 4 times to obtain the title compound in the form of a light red solid (14.89 g, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07320973B2 |
| Source dataset | uspto-grants-2008_01 |
| ORD ID | ord-298c72af63184d8bb9136bbd1b8f2387 |
| Source note | uspto-grants-2008_01 |