HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1688752Generated: October 30, 2026
HCID 178420675, compound → HCID 178438749, compound
https://huagongshe.com/reaction/1688752
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 178420675 | HCID 178420675 | — |
| Reactant | HCID 178438754 | HCID 178438754 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ammonium Chloride | HCID 25517 | — |
| Product | HCID 178438749 | HCID 178438749 | — |
Reaction Steps
To a solution of ethyl [(trans-3-{6-[(2′-cyano-3-fluorobiphenyl-4-yl)methyl]-2-methyl-5-oxo-7-propyl[1,2,4]triazolo[1,5-a]pyrimidin-4(5H)-yl}cyclobutyl)oxy]acetate (557 mg) in tetrahydrofuran (5 mL) was added 1 M methylmagnesium bromide-tetrahydrofuran solution (5 mL), and the mixture was stirred at room temperature for 15 hr. The reaction mixture was diluted with saturated aqueous ammonium chloride solution, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel chromatography [eluent: hexane/ethyl acetate=65/35→40/60 (volume ratio)] to give the title compound as a colorless amorphous compound (437 mg, 80%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08148383B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-898ca6984f514fa7a2f6b2c237e30aee |
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| Source note | uspto-grants-2012_04 |
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