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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1387408Generated: October 31, 2026

Water → 6-Aminoquinoline-5-carbohydrazide

https://huagongshe.com/reaction/1387408

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHydrazineHCID 9321—
ReactantHCID 178514317HCID 178514317—
Product6-Aminoquinoline-5-carbohydrazideHCID 45116988—

Reaction Conditions

Temperature145 °C

Reaction Steps

1-Hydrazono-1,3-dihydro-pyrrolo[3,2-f]quinoline-2-one (1.07 g, 5.05 mmol) was combined with 6.0 mL of anhydrous hydrazine and 5.0 mL of water in a 100 mL flask (oversize to allow for foaming) and heated at reflux (145° C. oil bath) under a condenser and nitrogen atmosphere, with stirring. After 4.5 hr, analytical HPLC showed that all of the hydrazone had been consumed. The reaction was cooled, diluted with 75 mL of water, and filtered to give 0.45 g (air dried) of 6-aminoquinoline-5-carboxylic acid hydrazide as an olive brown solid. Mass spectrum (negative ion electrospray): m/z=215 (100%). NMR (DMSO-d6): δ3.64 (s, 2H), 4.22 (s, 2H), 5.66 (s, 2H), 7.25 (d, 1H, J=9.1 Hz), 7.34 (m, 1H), 7.65 (d, 1H, J=9 Hz), 8.34 (d, 1H, J=8.5 Hz), 8.50 (s, 1H), 9.27 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06268391B1
Source datasetuspto-grants-2001_07
ORD IDord-0e451ad023b640eea48bc590390cceb3
Source noteuspto-grants-2001_07