HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1688563Generated: November 1, 2026
Hydrochloric Acid → HCID 178438633, compound
https://huagongshe.com/reaction/1688563
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Reactant | HCID 178438672 | HCID 178438672 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178438633 | HCID 178438633 | 69% |
Reaction Steps
2-[(trans-4-{6-[(2′-Cyanobiphenyl-4-yl)methyl]-5-oxo-7-propyl[1,2,4]triazolo[1,5-a]pyrimidin-4(5H)-yl}cyclohexyl)oxy]-N-methoxy-N-methylacetamide (0.75 g) was dissolved in tetrahydrofuran (10 mL), and methylmagnesium bromide (1.0 M tetrahydrofuran solution, 4 mL) was added at room temperature. The reaction mixture was warmed to 70° C. and stirred for 3 hr. 1 N Hydrochloric acid was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The obtained ethyl acetate layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography to give the title compound as a colorless solid (0.48 g, 69%).
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-f41c1180322147efadbff4a071d192a0 |
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| Source note | uspto-grants-2012_04 |
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