HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1688749Generated: October 30, 2026
HCID 178420675, compound → HCID 178438736, compound
https://huagongshe.com/reaction/1688749
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 178420675 | HCID 178420675 | — |
| Reactant | HCID 178438739 | HCID 178438739 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ammonium Chloride | HCID 25517 | — |
| Product | HCID 178438736 | HCID 178438736 | — |
Reaction Steps
To a solution of 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}-N-methoxy-N-methylcyclobutanecarboxamide (1.90 g) in tetrahydrofuran (5 mL) was added 1 M methylmagnesium bromide-tetrahydrofuran solution (5.3 mL), and the mixture was stirred at room temperature for 3 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=70/30→50/50 (volume ratio)] to give the title compound as a colorless amorphous compound (1.38 g, 79%).
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-f0753ce760a844b2a438ccee96fa7f74 |
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| Source note | uspto-grants-2012_04 |
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