HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1628903Generated: October 31, 2026
HCID 57786105, compound → HCID 57785833, compound
https://huagongshe.com/reaction/1628903
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 57786105 | HCID 57786105 | — |
| Reactant | HCID 178418797 | HCID 178418797 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ammonium Chloride | HCID 25517 | — |
| Product | HCID 57785833 | HCID 57785833 | — |
Reaction Steps
To a suspension of 9-chloro-1-(2,4-dichloro-6-methylphenyl)-1,2,3,4-tetrahydropyrimido[1,2-a]benzimidazole-6-carbaldehyde (150 mg, 0.380 mmol) in tetrahydrofuran (3.8 mL) was added dropwise 3-butenylmagnesium bromide (ca. 0.8 M solution in diethyl ether, 0.900 mL) at 0° C., and the mixture was stirred at room temperature for 30 min. The reaction mixture was diluted with aqueous saturated ammonium chloride, and extracted with ethyl acetate. The combined organic layer was washed with brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel eluting with a 10-50% ethyl acetate/n-hexane gradient mixture to give the two title compounds as colorless solids.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08785460B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-34697011ad0743a1bb6a4a4b6a57a3d1 |
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| Source note | uspto-grants-2014_07 |
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