Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 129457Generated: October 29, 2026

1-(2-Hydroxyethyl)piperazine → HCID 19035980, compound

https://huagongshe.com/reaction/129457

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Hydroxyethyl)piperazineHCID 7677—
ReactantHCID 19035982HCID 19035982—
ProductHCID 19035980HCID 1903598036.4%

Reaction Steps

9-Chloro-9H-indeno[1,2-b]pyrazine-2,3(1H, 4H)-dione (3.0 g, 12.8 mmol) was reacted with N-(2-hydroxyethyl)piperazine (3.66 g, 28.2 mmol) as described in example 18. The crude product was purified by dissolving in aqueous NaHCO3 /NaOH and precipitated by adding to hydrochloric acid. The procedure was repeated and the product was finally washed with ethanol and dried to give 1.53 g (28%) of the title compound as a dihydrochloride. M.p. 210° C. (destruction). 1H-NMR (DMSO-d6 +D2O, δ): 2.35-3.6 (m, 10H), 3.75 (m, 2H), 4.73 (s, 1H), 7.22 (t, 1H), 7.35 (t, 1H), 7.51 (d,1H), 7.57 (d, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05468748
Source datasetuspto-grants-1995_11
ORD IDord-df0c434133554b388a1635728eccd17e
Source noteuspto-grants-1995_11