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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1690627Generated: November 1, 2026

Sodium → HCID 178457607, compound

https://huagongshe.com/reaction/1690627

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodiumHCID 5360545—
ReactantHCID 66906304HCID 66906304—
ReactantDichloromethane brineHCID 131726697—
ReactantPropylguanidine hydrochlorideHCID 178457588—
SolventEthanolHCID 702—
SolventDimethylformamideHCID 6228—
ProductHCID 178457607HCID 17845760735%

Reaction Steps

Sodium (0.15 g, 6.5 mmol) was dissolved in ethanol (3.5 mL) at room temperature. Once all the sodium was dissolved, propylguanidine hydrochloride (0.65 g, 6.5 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)carbonyl]biphenyl-4-yl}-3-methylbutanoate (0.51 g, 1.0 mmol) and DMF (3.5 mL) was added at room temperature. The mixture was stirred at 50° C. until reaction was completed. The mixture was then 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, 4 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 0.20 g (35%) of the desired product as a white solid: mp=99° C.; 1H NMR (400 MHZ, d6-DMSO) δ 12.22 (bs, 1H), 11.15 (bs, 1H), 9.02 (t, 1H), 8.69 (bs, 1H), 7.58 (m, 4H), 7.30 (d, 1H), 7.15 (s, 1H), 7.09 (d, 1H), 4.08 (t, 2H), 3.38 (t, 2H), 3.21 (m, 10H), 3.18 (s, 3H), 2.81 (s, 2H), 2.73 (s, 3H), 1.86 (m, 2H), 1.49 (m, 2H), 1.41 (s, 6H), 0.87 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153647B2
Source datasetuspto-grants-2012_04
ORD IDord-90b4d6ef6ad64e2691aab47ebff8929f
Source noteuspto-grants-2012_04