HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2048498Generated: November 1, 2026
HCID 178420675, compound → HCID 178438623, compound
https://huagongshe.com/reaction/2048498
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 178420675 | HCID 178420675 | — |
| Reactant | HCID 178438633 | HCID 178438633 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ammonium Chloride | HCID 25517 | — |
| Product | HCID 178438623 | HCID 178438623 | — |
Reaction Steps
To a solution of 4′-({5-oxo-4-[trans-4-(2-oxopropoxy)cyclohexyl]-7-propyl-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl}methyl)biphenyl-2-carbonitrile (251 mg) in tetrahydrofuran (3 mL) was added 1 M methylmagnesium bromide-tetrahydrofuran solution (1 mL), and the mixture was stirred at room temperature for 16 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 basic silica gel chromatography [eluent: hexane/ethyl acetate=70/30→40/60 (volume ratio)] to give the title compound as a colorless amorphous compound (237 mg, 91%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08592431B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-2eda21000651469c99e24680e8c7d69a |
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| Source note | uspto-grants-2013_11 |
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