Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1043868Generated: October 31, 2026

Benzoylhydrazine → HCID 53258710, compound

https://huagongshe.com/reaction/1043868

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoylhydrazineHCID 11955—
Reactant5,6-Dihydro-4H-pyrrolo[3,2,1-ij]quinoline-1-carboxylic acidHCID 22556886—
ProductHCID 53258710HCID 53258710—

Reaction Steps

2-(5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinolin-1-yl)-5-phenyl-1,3,4-oxadiazole was synthesized as outlined in General Procedure J using 5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinoline-1-carboxylic acid and benzohydrazide. The crude product was purified using reverse phase chromatography (HPLC, C-18) using trifluoroacetic acid as a modifier to give the desired product 2-(5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinolin-1-yl)-5-phenyl-1,3,4-oxadiazole as a yellow solid. Mp=155-157° C.; 400 MHz 1HNMR (DMSO-d6) δ 8.31 (s, 1H), 8.13-8.10 (m, 2H), 7.90 (d, J=8.0 Hz, 1H), 7.65-7.63 (m, 3H), 7.21 (t, J=6.8 Hz, 1H), 7.06 (d, J=7.6 Hz, 1H), 4.31 (t, J=5.6 Hz, 2H), 2.99 (t, J=6.0 Hz, 2H), 2.21-2.18 (m, 2H); LCMS [M+H]: 302.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563567B2
Source datasetuspto-grants-2013_10
ORD IDord-2ca3aa98d6bd48c7868279e8c7ca0e4a
Source noteuspto-grants-2013_10