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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 131446Generated: October 31, 2026

(S)-2-(2-Methoxyethyl)piperazine → HCID 10317297, compound

https://huagongshe.com/reaction/131446

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-2-(2-Methoxyethyl)piperazineHCID 55287560—
ReactantHCID 58625885HCID 58625885—
SolventIsopropanolHCID 3776—
ProductAmmonium HydroxideHCID 14923—
ProductHCID 10317297HCID 10317297177.7%

Reaction Conditions

Temperature81.5 °C

Reaction Steps

Stir 6-fluoro-2-methyl-10-methylsulfanyl-4H-3-thia-4,9-diaza-benzo[f]azulene (3.40 g, 12.2 mmol) and (S)-2-(2-methoxy-ethyl)-piperazine (2.20 g, 15.3 mmol) in isopropyl alcohol (20 mL) at ambient temperature under nitrogen for 20-30 minutes to dissolve. Heat to reflux (80-83° C.) for 3-4 days, and then allow cooling to ambient temperature. Concentrate the mixture under reduced pressure to give a residue. Purify the residue by flash chromatography, eluting with 90:10:1→80:20:1/EtOAc:MeOH:c. NH4OH to give 4.06 g (89%) the title compound. 1H NMR (400 MHz, DMSO-d6) δ 7.75 (bs, 1H), 6.78 (m, 1H), 6.68 (m, 1H), 6.53 (m, 1H), 6.35 (s, 1H), 3.80 (m, 2H), 3.40 (m, 2H), 3.23 (s, 3H), 2.88 (m, 1H), 2.71 (m, 3H), 2.41 (m, 1H), 2.30 (bs, 1H), (s, 3H), 1.53 (m, 2H). HRMS (ES) exact mass M+H calcd for C19H23FN4OS 375.1655; found 375.1663.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07384934B2
Source datasetuspto-grants-2008_06
ORD IDord-26b3793ff3274a8ebaa5c81a94ed9efe
Source noteuspto-grants-2008_06