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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1435960Generated: October 27, 2026

1-Benzylpyrrolidin-3-yl methanesulfonate → (S)-6-(1-Benzylpyrrolidin-3-yloxy)-isoquinolin-1-ylamine

https://huagongshe.com/reaction/1435960

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzylpyrrolidin-3-yl methanesulfonateHCID 9899811—
Reactant2-tert-butylimino-N,N-diethyl-1-methyl-1,3,2lambda5-diazaphosphinan-2-amineHCID 19990018—
Reactant1-Aminoisoquinolin-6-olHCID 135753991—
SolventAcetonitrileHCID 6342—
Product(S)-6-(1-Benzylpyrrolidin-3-yloxy)-isoquinolin-1-ylamineHCID 6887497040.1%

Reaction Conditions

Temperature110 °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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07618985B2
Source datasetuspto-grants-2009_11
ORD IDord-f1eb9e119b2b4a98a2767c23c61efedf
Source noteuspto-grants-2009_11