HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2369349Generated: October 31, 2026
Heptane → (8S)-2-{(E)-2-[6-methoxy-5-(4-methyl-1H-imidazol-1-yl)pyridin-2-yl]vinyl}-8-(2-trifluoromethylphenyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[1,5-a]pyridine di-D-tartrate
https://huagongshe.com/reaction/2369349
Participants
| Role | Name | HCID | Charge |
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| Reactant | Heptane | HCID 8900 | — |
| Reactant | D-Tartrate | HCID 5460284 | — |
| Reactant | E-2212 | HCID 46854987 | — |
| Solvent | D-tartaric acid ethanol | HCID 86653873 | — |
| Product | (8S)-2-{(E)-2-[6-methoxy-5-(4-methyl-1H-imidazol-1-yl)pyridin-2-yl]vinyl}-8-(2-trifluoromethylphenyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[1,5-a]pyridine di-D-tartrate | HCID 86659212 | — |
Reaction Steps
(8S)-2-{(E)-2-[6-methoxy-5-(4-methyl-1H-imidazol-1-yl)pyridin-2-yl]vinyl}-8-(2-trifluoromethylphenyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[1,5-a]pyridine (810.18 mg) was dissolved in 8 mL of a D-tartaric acid-ethanol solution (751.13 mg/10 mL) with stirring at room temperature. The oil was precipitated when 2 mL of heptane was added. Accordingly, the oily substance was dissolved by ultrasonic treatment to prepare a clear solution. Several mg of crystals of the 1.5 D-tartrate prepared according to Example 1 were added, followed by stirring at room temperature. Stirring for about one hour resulted in gelation and subsequent precipitation of a solid. Further, stirring was continued while gradually adding 14 mL of heptane. A part of the suspension (2 mL) was separated and the solid was collected by filtration through a glass filter. The solid was dried under reduced pressure at room temperature to obtain 71.14 mg of the title compound as white solid crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08703954B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-3d4cbf876ec44f7e8670bf079014ff90 |
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| Source note | uspto-grants-2014_04 |
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