HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Benzylpyrrolidin-3-yl methanesulfonate → (S)-6-(1-Benzylpyrrolidin-3-yloxy)-isoquinolin-1-ylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Benzylpyrrolidin-3-yl methanesulfonate | HCID 9899811 | — |
| Reactant | 2-tert-butylimino-N,N-diethyl-1-methyl-1,3,2lambda5-diazaphosphinan-2-amine | HCID 19990018 | — |
| Reactant | 1-Aminoisoquinolin-6-ol | HCID 135753991 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (S)-6-(1-Benzylpyrrolidin-3-yloxy)-isoquinolin-1-ylamine | HCID 68874970 | 40.1% |
Reaction Conditions
| Temperature | 110 °C |
|---|
Reaction Steps
1-Amino-6-hydroxyisoquinoline (50 mg, 0.312 mmol), prepared as described in WO 00/24718 (Akzo Nobel N.V.), and 2-tert-butylimino-2-diethylamino-1,3-dimethyl-perhydro-1,3,2-diazaphosphorine on polystyrene (284 mg, ˜2.2 mmol.g−1, ˜0.624 mmol) were stirred at ambient temperature in acetonitrile (4 ml) for 15 min. (R) Methanesulfonic acid 1-benzylpyrrolidin-3yl ester (0.312 mmol) was added and the mixture heated to 110° C. and stirred for 60 h. The mixture was filtered and the precipitate washed with acetonitrile. The filtrate was concentrated and then purified by prep-HPLC to give (S)-6-(1-Benzylpyrrolidin-3-yloxy)-isoquinolin-1-ylamine (40 mg),
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07618985B2 |
| Source dataset | uspto-grants-2009_11 |
| ORD ID | ord-f1eb9e119b2b4a98a2767c23c61efedf |
| Source note | uspto-grants-2009_11 |