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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 715714Generated: October 31, 2026

Diisopropylamine → HCID 53341080, compound

https://huagongshe.com/reaction/715714

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantHCID 24950198HCID 24950198—
ReactantHCID 58071886HCID 58071886—
SolventDimethylacetamideHCID 31374—
ProductHCID 53341080HCID 53341080—

Reaction Conditions

Temperature70 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187478B2
Source datasetuspto-grants-2015_11
ORD IDord-adc6104c22bf420088bc9a7bd271fa35
Source noteuspto-grants-2015_11