HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35348Generated: October 28, 2026
2,3-Dihydroxybutanedioic Acid → 2,3-Dihydroxybutanedioate
https://huagongshe.com/reaction/35348
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,3-Dihydroxybutanedioic Acid | HCID 875 | — |
| Reactant | 3-(aminocarbonyl)-4-[4,4-bis(4-fluorophenyl)butyl]-N-(2,6-dimethylphenyl)-1-piperazineacetamide | HCID 14230088 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2,3-Dihydroxybutanedioate | HCID 3806114 | — |
| Product | 3-(aminocarbonyl)-4-[4,4-bis(4-fluorophenyl)butyl]-N-(2,6-dimethylphenyl)-1-piperazineacetamide | HCID 14230088 | — |
Reaction Steps
To a stirred solution of 3 parts of 3-(aminocarbonyl)-4-[4,4-bis(4-fluorophenyl)butyl]-N-(2,6-dimethylphenyl)-1-piperazineacetamide in 24 parts of ethanol was added a solution of 0.94 parts of (+)-2,3-dihydroxybutanedioic acid in 24 parts of ethanol. The whole was evaporated and the oily residue was dissolved in warm 4-methyl-2-pentanone. After cooling to 0° C., the product was filtered off and dissolved in 2-propanone. 0.2 Parts of 2,3-dihydroxybutanedioic acid were added and upon the addition of 4-methyl-2-pentanone, the product was precipitated. It was filtered off and dried, yielding 0.8 parts of (+)-3-(aminocarbonyl)-4-[4,4-bis(4-fluorophenyl)butyl]-N-(2,6-dimethylphenyl)-1-piperazineacetamide [R-(R*,R*)]-2,3-dihydroxybutanedioate (2:3) monohydrate; mp. 78.1° C. (compound 173).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04766125 |
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| Source dataset | uspto-grants-1988_08 |
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| ORD ID | ord-a74d9d077e6941f5a1586fa85bdf3173 |
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| Source note | uspto-grants-1988_08 |
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