Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Succinic Acid | HCID 1110 | — |
| Reactant | Batefenterol | HCID 10372836 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Batefenterol Succinate | HCID 16718568 | 41.8% |
Reaction Steps
Ethanol (14 ml) was added to Biphenyl-2-ylcarbamic acid 1-[2-(2-chloro-4-{[(R)-2-hydroxy-2-(8-hydroxy-2-oxo-1,2-dihydroquinolin-5-yl)ethylamino]methyl}-5-methoxyphenylcarbamoyl)-ethyl]piperidin-4-yl ester (1.5 g) and heated at ˜70° C. for 1 h. The temperature was then lowered to 50° C. and succinic acid (251.25 mg, 1.05 equiv) in ethanol (2 ml) was added portionwise over approximately 4 hours. After all the acid was added, water (2.25 ml) was added, followed by a further 30 min at 50° C. The reaction was then temperature cycled between 0° C. and 40° C. over 3 days. The resulting white solid was isolated by filtration, washed with ethanol and dried in a vacuum oven at ambient temperature, to provide the title compound as a crystalline solid (727 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07960551B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-193ddf90a01945a4b5d5b3268937dd7c |
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| Source note | uspto-grants-2011_06 |
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