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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1694574Generated: October 31, 2026

Isopropyl Acetate → (R)-N-(pyrrolidin-3-yl)isoquinolin-5-amine

https://huagongshe.com/reaction/1694574

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropyl AcetateHCID 7915—
Reactant(r)-Tert-butyl 3-(isoquinolin-5-ylamino)pyrrolidine-1-carboxylate dibenzoyl-d-tartaric acid saltHCID 131729631—
SolventSodium HydroxideHCID 14798—
Product(R)-N-(pyrrolidin-3-yl)isoquinolin-5-amineHCID 44594455—

Reaction Steps

To a 5 L flask equipped with a mechanical stirrer and an internal temperature probe were added (R)-tert-butyl 3-(isoquinolin-5-ylamino)pyrrolidine-1-carboxylate dibenzoyl-D-tartaric acid salt (180 g, 0.27 mol, from Example 2) and 2.7 L of isopropyl acetate. The suspension was stirred while 630 mL of 1N sodium hydroxide was added maintaining an internal reaction temperature below 30° C. Stirring was continued until a biphasic solution was obtained. The aqueous layer was removed and the remaining organic layer was washed with 1N sodium hydroxide (360 mL) and water (360 mL). Five normal HCl (215 mL) was added and the reaction was stirred until all (R)-tert-butyl 3-(isoquinolin-5-ylamino)pyrrolidine-1-carboxylate was consumed. The pH of the reaction was adjusted to >12 with 270 mL of 5N sodium hydroxide. The layers were separated. The pH of the aqueous layer was adjusted to >12 with 50 mL 5 N NaOH. The aqueous layer was re-extracted with 1.5 L of isopropyl acetate. The combined organic layers were concentrated to a volume of 770 mL.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158796B2
Source datasetuspto-grants-2012_04
ORD IDord-7a8dd76341f34d8f86a6fcd53d302a07
Source noteuspto-grants-2012_04