HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2407668Generated: October 30, 2026
Diisopropylethylamine → HCID 58504166, compound
https://huagongshe.com/reaction/2407668
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-(Chloromethyl)-5-phenyl-1,3,4-oxadiazole | HCID 314941 | — |
| Reactant | HCID 66989233 | HCID 66989233 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 58504166 | HCID 58504166 | — |
Reaction Steps
2-(Chloromethyl)-5-phenyl-1,3,4-oxadiazole (31 mg, prepared according to the reported preparation in Natero, R.; et al. Synth. Commun. 2004, 34, 2523) was added to a solution of the compound prepared in Example 11 (60 mg) and diisopropylethylamine (0.083 mL) in N,N-dimethylformamide (0.8 mL). The solution was heated to 100° C. overnight. The reaction was cooled to room temperature, diluted with ethyl acetate and washed twice with a saturated aqueous sodium bicarbonate solution. The organic phase was dried over anhydrous magnesium sulfate and concentrated. The residue was purified by column chromatography on silica gel (ethyl acetate:hexane=1:1, then ethyl acetate) to obtain the title compound (36 mg) having the following physical data.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08809538B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-c756b914f445429eb093d42db261b960 |
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| Source note | uspto-grants-2014_08 |
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