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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Di-benzoyl-d-tartaric acid | HCID 12362977 | — |
| Reactant | Tert-butyl 3-(isoquinolin-5-ylamino)pyrrolidine-1-carboxylate | HCID 23079381 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | (r)-Tert-butyl 3-(isoquinolin-5-ylamino)pyrrolidine-1-carboxylate dibenzoyl-d-tartaric acid salt | HCID 131729631 | 44.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08158796B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-69f56cc0ae4d4bd4a24a68d9b656055b |
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| Source note | uspto-grants-2012_04 |
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