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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1694573Generated: October 30, 2026

Di-benzoyl-d-tartaric acid → (r)-Tert-butyl 3-(isoquinolin-5-ylamino)pyrrolidine-1-carboxylate dibenzoyl-d-tartaric acid salt

https://huagongshe.com/reaction/1694573

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDi-benzoyl-d-tartaric acidHCID 12362977—
ReactantTert-butyl 3-(isoquinolin-5-ylamino)pyrrolidine-1-carboxylateHCID 23079381—
SolventIsopropanolHCID 3776—
Product(r)-Tert-butyl 3-(isoquinolin-5-ylamino)pyrrolidine-1-carboxylate dibenzoyl-d-tartaric acid saltHCID 13172963144.9%

Reaction Conditions

Temperature42 °C

Reaction Steps

Salt Formation: To a 5 L flask equipped with an internal temperature probe, a heating mantle and a mechanical stirrer were added tert-butyl 3-(isoquinolin-5-ylamino)pyrrolidine-1-carboxylate (250 g, 0.798 mol, from Example 1) and 3 L of 2-propanol. The mixture was stirred and warmed to 42° C. to form a homogeneous solution. To the stirred solution was added dibenzoyl-D-tartaric acid (D-DBTA) (242.9 g, 0.678 mol) in one portion and another 0.9 L of 2-propanol. The mixture was stirred at 40° C. for 15 minutes to form a solution. The mixture was stirred at 40° C. to form a yellow slurry. The slurry was cooled to 30° C. The suspension was filtered, washed with 2×250 mL of 2-propanol and dried in a vacuum oven at ˜35° C. Approximately 204.3 g of (R)-tert-butyl 3-(isoquinolin-5-ylamino)pyrrolidine-1-carboxylate dibenzoyl-D-tartaric acid salt crude product was obtained as a yellow solid (84% ee, 38% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158796B2
Source datasetuspto-grants-2012_04
ORD IDord-69f56cc0ae4d4bd4a24a68d9b656055b
Source noteuspto-grants-2012_04