HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → 4-(1-Chloro-5-isoquinolyl)aminopiperidine trifluoroacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 4-(1-Chloro-5-isoquinolyl)amino-1-(tert-butoxycarbonyl)piperidine | HCID 21979829 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(1-Chloro-5-isoquinolyl)aminopiperidine trifluoroacetate | HCID 21979875 | — |
Reaction Steps
Deprotection was performed (room temperature, 2 hours) by using Intermediate 84 (81.9 mg) and a mixed solution of trifluoroacetic acid and methylene chloride (1:1, 2 ml). The solvent was evaporated under reduced pressure, and the residue was added with methanol (2 ml) and diethyl ether (6 ml). The deposited precipitates were collected by filtration and washed with diethyl ether to obtain the title compound (64 mg) as yellow powdery crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07094789B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-c7ab94fd6f5a4dc4b97d834fc0e5f2b3 |
| Source note | uspto-grants-2006_08 |