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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 131516Generated: November 1, 2026

(S)-2-(2-Methoxyethyl)piperazine → HCID 135464320, compound

https://huagongshe.com/reaction/131516

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-2-(2-Methoxyethyl)piperazineHCID 55287560—
ReactantHCID 136384186HCID 136384186—
ProductHCID 135464320HCID 13546432018%

Reaction Conditions

Temperature115 °C

Reaction Steps

Following the method of Example 380 using 8-fluoro-11H-12-thia-6,11-diaza-dibenzo[a,f]azulen-5-ylamine hydrochloride (0.40 g, 1.3 mmol) and (S)-2-(2-methoxy-ethyl)-piperazine (0.36 g, 2.5 mmol), stirring at 115° C. for 24 hours, wash the separated organic layer with 0.1 N NaOH (2×), and extract the combined aqueous layers with ethyl acetate. Combine the organics and wash with a saturated solution of sodium chloride (3×), and then dry (sodium sulfate), filter, and concentrate under reduced pressure to a residue. Purify the residue by flash chromatography, eluting with a gradient of a solution of 5% 2M ammonia in methanol, in dichloromethane (in dichloromethane) to give the title compound (0.096 g). Mass spectrum (APCI+, m/e): 411 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07384934B2
Source datasetuspto-grants-2008_06
ORD IDord-e5168557bd974ef3b553ae5ca2058bd5
Source noteuspto-grants-2008_06