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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1895828Generated: October 31, 2026

Hydrazine → HCID 175538, compound

https://huagongshe.com/reaction/1895828

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazineHCID 9321—
Reactant1-(3-Phthalimido-2-hydroxy propyl)-2-nitroimidazoleHCID 337334—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 175538HCID 17553883.3%

Reaction Steps

Compound 8 (5 g, 15.8 mmol) was added to a solution of pure hydrazine (608 mg, 18.97 mmol, 1.2 equivalent) in 50 ml of ethyl alcohol and 4 ml of water. The mixture was refluxed for 2 h and then held at room temperature. The white solid (phthalhydrazide) was filtered. The filtrate was concentrated and the residue was redistributed in ethyl acetate and water. The water phase was extracted two times with ethyl acetate and the combined ethyl acetate phase was dried to give a yellowish solid as the HCl salt (9, 2.45 g, 70% yield). 1H NMR (D2O, δppm) (HCl salt): 2.91 (dd, 1H, NH2—CHa, J=13.2 Hz, 9.9 Hz), 3.21 (dd, 1H, NH2—CHb, J=13.2 Hz, 2.7 Hz), 4.19 (tt, 1H, HO—CH—, J=9.0 Hz, 3.0 Hz), 4.28 (dd, 1H, imidazole-CHa—, J=13.8 Hz, 8.7 Hz), 4.57 (dd, 1H, imidazole-CHb—, J=13.8 Hz, 2.7 Hz), 7.09 (d, 1H, J=0.9 Hz, —CH═), 7.35 (d, 1H, J=0.9 Hz, —CH═). 13C NMR (D2O, δppm). 42.06, 53.00, 66.86, 128.06, 128.92, 144.73.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08518371B2
Source datasetuspto-grants-2013_08
ORD IDord-a2e4868a8be8457cb368e31c8abaee5b
Source noteuspto-grants-2013_08