HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473305Generated: October 31, 2026
2,3-Dihydroxybutanedioic Acid → L-Tartaric acid
https://huagongshe.com/reaction/473305
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,3-Dihydroxybutanedioic Acid | HCID 875 | — |
| Reactant | Ilorasertib | HCID 46207586 | — |
| Solvent | Oxolane--water (1/1) | HCID 21881883 | — |
| Product | L-Tartaric acid | HCID 444305 | — |
Reaction Steps
A saturated solution of l-tartaric acid was prepared at 25 C by dissolving tartaric acid in a 85/15 v/v THF/water mixture. This solution (2 mL) was heated 2 to 65 C. Approximately 200 mg of N-(4-{4-amino-7-[1-(2-hydroxyethyl)-1H-pyrazol-4-yl]thieno[3,2-c]pyridin-3-yl}phenyl)-N′-(3-fluorophenyl)urea free base solid was then added, which readily dissolved. N-(4-{4-amino-7-[1-(2-hydroxyethyl)-1H-pyrazol-4-yl]thieno[3,2-c]pyridin-3-yl}phenyl)-N′-(3-fluorophenyl)urea L-bitartrate crystallized within 30 minutes from this clear solution. The slurry was then diluted with the saturated solution (at 25° C.) of l-tartaric acid and cooled to ambient temperatures. The slurry was continue to be stirred overnight and the solids were isolated via filtration. The filtered solids were washed with 85/15 v/v mixture of THF/water to remove excess l-tartaric acid and then dried in the oven at 45° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08633317B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-778fb59ef0a3477da7892785237e6397 |
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| Source note | uspto-grants-2014_01 |
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