Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518269Generated: November 2, 2026

(S)-(9H-fluoren-9-yl)methyl 1-(8-chloro-1-(tetrahydro-2H-pyran-4-ylcarbamoyl)isoquinolin-3-yl)ethylcarbamate → (S)-3-(1-aminoethyl)-8-chloro-N-(tetrahydro-2H-pyran-4-yl)isoquinoline-1-carboxamide

https://huagongshe.com/reaction/518269

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-(9H-fluoren-9-yl)methyl 1-(8-chloro-1-(tetrahydro-2H-pyran-4-ylcarbamoyl)isoquinolin-3-yl)ethylcarbamateHCID 69097730—
SolventMorpholineHCID 8083—
Product(S)-3-(1-aminoethyl)-8-chloro-N-(tetrahydro-2H-pyran-4-yl)isoquinoline-1-carboxamideHCID 69097729—

Reaction Conditions

Temperature45 °C

Reaction Steps

(S)-(9H-fluoren-9-yl)methyl 1-(8-chloro-1-(tetrahydro-2H-pyran-4-ylcarbamoyl)isoquinolin-3-yl)ethylcarbamate (351) (20.0 g, 36.0 mmol, 1.0 eq) was suspended in morpholine (200 mL), and then stirred at 40-50° C. for 1 h. The reaction mixture was concentrated in vacuo and then 1,4-dioxane (200 mL) was added to the residue. The mixture was concentrated in vacuo. The operation was repeated for 3-4 times. The residue was purified by flash column chromatography on silica gel (2-10% MeOH-DCM) to afford (S)-3-(1-aminoethyl)-8-chloro-N-(tetrahydro-2H-pyran-4-yl)isoquinoline-1-carboxamide (352).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115141B2
Source datasetuspto-grants-2015_08
ORD IDord-5d67c3ba02374b94a7d609af491d3fa9
Source noteuspto-grants-2015_08