HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 870544Generated: October 29, 2026
Diisopropylamine → HCID 53341080, compound
https://huagongshe.com/reaction/870544
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | HCID 24950198 | HCID 24950198 | — |
| Reactant | HCID 58071886 | HCID 58071886 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 53341080 | HCID 53341080 | — |
Reaction Steps
97 mg Trifluoromethanesulfonic acid 7-(3,4-dimethoxy-phenyl)-[1,6]naphthyridine-5-yl ester (6.2), 30 mg 5-aminomethyl-3H-[1,3,4]oxadiazole-2-one (2.33) and 0.132 mL N,N-diisopropylamine were placed in dimethylacetamide at ambient temperature. The reaction was heated to 70° C. overnight. After this time the reaction was cooled to ambient temperature and additional 0.132 mL N,N-diisopropylamine were added. The reaction was heated to 90° C. for 6 h. After this time, the mixture was cooled to ambient temperature and partitioned between water and ethyl acetate. The organic phase was separated and the aqueous phase was extracted with additional ethyl acetate (×3) and the combined organic fractions were dried over sodium sulfate, filtered and the solvent was concentrated from the filtrate under reduced pressure. Purification by and then by silica gel chromatography (ethyl acetate/methanol: 100:0 to 95:5) provided the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08969568B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-777f4548bd5948fba477c98ebbeb9172 |
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| Source note | uspto-grants-2015_03 |
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