HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 519755Generated: October 27, 2026
HCID 178420675, compound → HCID 178438634, compound
https://huagongshe.com/reaction/519755
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 178420675 | HCID 178420675 | — |
| Reactant | HCID 178438656 | HCID 178438656 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ammonium Chloride | HCID 25517 | — |
| Product | HCID 178438634 | HCID 178438634 | — |
Reaction Steps
To a solution of 4′-({5-oxo-4-[trans-4-(2-oxoethoxy)cyclohexyl]-7-propyl-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl}methyl)biphenyl-2-carbonitrile (841 mg) in tetrahydrofuran (15 mL) was added 1 M methylmagnesium bromide-tetrahydrofuran solution (2.2 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 basic silica gel chromatography [eluent: hexane/ethyl acetate=70/30→40/60 (volume ratio)] to give the title compound as a colorless amorphous compound (387 mg, 76%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09115136B2 |
|---|
| Source dataset | uspto-grants-2015_08 |
|---|
| ORD ID | ord-c7c4c30c5b3e45bbbc47192712ed7883 |
|---|
| Source note | uspto-grants-2015_08 |
|---|