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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1690618Generated: October 31, 2026

Guanidine Hydrochloride → HCID 178495365, compound

https://huagongshe.com/reaction/1690618

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGuanidine HydrochlorideHCID 5742—
ReactantSodiumHCID 5360545—
ReactantEthyl 3-{2-(3-methoxypropoxy)-4'-[(4-methylpiperazin-1-yl)carbonyl]biphenyl-4-yl}propanoateHCID 66906577—
ReactantDichloromethane brineHCID 131726697—
SolventEthanolHCID 702—
SolventDimethylformamideHCID 6228—
ProductHCID 178495365HCID 17849536545%

Reaction Steps

Sodium (0.11 g, 4.8 mmol) was dissolved in ethanol (2.5 mL) at room temperature. Once all the sodium was dissolved, guanidine hydrochloride (0.46 g, 4.8 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}propanoate (0.36 g, 0.8 mmol) and DMF (2.5 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, 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 0.19 g (45%) of the desired product as a white solid: mp=122° C.; 1H NMR (400 MHZ, d6-DMSO) δ 12.13 (bs, 1H), 11.15 (bs, 1H), 8.29 (bs, 2H), 7.52 (m, 4H), 7.25 (d, 1H), 7.02 (s, 1H), 6.92 (d, 1H), 4.00 (t, 2H), 3.31 (t, 2H), 3.30 (m, 4H), 3.20 (s, 3H), 2.89 (m, 8H) 2.72 (s, 3H), 1.84 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153647B2
Source datasetuspto-grants-2012_04
ORD IDord-2920769776664ff284088fa0b72a734b
Source noteuspto-grants-2012_04