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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1690612Generated: October 31, 2026

Sodium → HCID 178449227, compound

https://huagongshe.com/reaction/1690612

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodiumHCID 5360545—
ReactantEthyl 3-{2-(3-methoxypropoxy)-4'-[(4-methylpiperazin-1-yl)methyl]biphenyl-4-yl}propanoateHCID 66906778—
ReactantDichloromethane brineHCID 131726697—
ReactantHCID 178449217HCID 178449217—
SolventEthanolHCID 702—
SolventDimethylformamideHCID 6228—
ProductHCID 178449227HCID 17844922753%

Reaction Steps

Sodium (0.31 g, 13.5 mmol) was dissolved in ethanol (7 mL) at room temperature. Once all the sodium was dissolved, 1-butylguanidine hydrochloride (2.05 g, 13.5 mmol) was added and the mixture was stirred for 1 h. A white precipitate formed and was filtered off. The filtrate was evaporated under reduced pressure and a solution of ethyl 3-{2-(3-methoxypropoxy)-4′-[(4-methylpiperazin-1-yl)methyl]biphenyl-4-yl}propanoate (0.98 g, 2.2 mmol) and DMF (7 mL) was added at room temperature. After completion of the reaction, the mixture was poured into dichloromethane/brine (50/50). The aqueous layer was extracted three times with dichloromethane. The combined organic layers were washed with brine, dried over anhydrous sodium sulfate, filtered and evaporated under reduced pressure. The residue was then dissolved in ethanol and HCl in diethyl ether (1N, 8 mL) was added. The mixture was evaporated and the residue was purified on reverse phase (C18) flash chromatography (H2O, HCl N/1000, acetonitrile, 100/0 to 80/20) to afford 0.60 g (53%) of the desired product as a white solid: mp=125° C.; 1H NMR (400 MHZ, d6-DMSO) δ 9.05 (bs, 1H), 8.70 (bs, 2H), 7.55 (en, 4H), 7.25 (d, 1H), 7.08. (s, 1H), 7.90 (d, 1H), 4.30 (s, 2H), 4.04 (t, 2H), 3.36 (m, 10H), 3.21 (t, 2H), 3.19(s, 3H), 2.86 (m, 4H), 2.81 (s, 3H), 1.97 (m, 2H), 1.45 (m, 2H), 1.30 (m, 2H), 0.85 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153647B2
Source datasetuspto-grants-2012_04
ORD IDord-ee2d589d20844e5394321c65e8852ba1
Source noteuspto-grants-2012_04