HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 519520Generated: October 31, 2026
HCID 178418573, compound → HCID 178438718, compound
https://huagongshe.com/reaction/519520
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Reactant | HCID 178438729 | HCID 178438729 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178438718 | HCID 178438718 | — |
Reaction Steps
tert-Butyl 2-[(trans-4-{6-[(2′-cyano-3-fluorobiphenyl-4-yl)methyl]-5-oxo-7-propyl[1,2,4]triazolo[1,5-a]pyrimidin-4(5H)-yl}cyclohexyl)oxy]propanoate (548 g) was dissolved in tetrahydrofuran (2.7 L), and methylmagnesium bromide (1.0 M tetrahydrofuran solution, 3.5 L) was added with the internal temperature maintained below 10° C. The reaction mixture was stirred at the same temperature for 1 hr, and partitioned among saturated aqueous ammonium chloride solution (600 mL), water (600 mL) and ethyl acetate (500 mL). The aqueous layer was extracted with ethyl acetate (1 L). The combined extracts were washed with saturated brine (1 L), dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography to give the title compound as a racemate (428 g, 84%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09115136B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-1050d0e9895f4706ba6ed26bb417af5f |
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| Source note | uspto-grants-2015_08 |
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