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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 577700Generated: October 26, 2026

Hydrochloric Acid → HCID 178480794, compound

https://huagongshe.com/reaction/577700

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 2-cyano-4,4-diethoxybutyrateHCID 4151505—
ReactantHCID 178481028HCID 178481028—
ReactantHCID 178501943HCID 178501943—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
ProductHCID 178480794HCID 17848079443.5%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of crude 1-(1-methyl-1H-pyrazol-4-yl)guanidine (17.5 g, crude) and ethyl 2-cyano-4,4-diethoxybutanoate (13.08 g, 0.06 mol) in EtOH (50 mL) was added CH3ONa/CH3OH (150 mL, 0.06 mol) at 20° C., and the reaction mixture was stirred at 100° C. for 20 hrs. The pH was adjusted to 2 by HCl (6 M) and stirred for 30 min. Then pH was adjusted to 7-8 by aqueous NaOH (1 M). The reaction mixture was filtered and the filter cake was dried in vacuo to afford a first batch of pure product. The filtrate was concentrated in vacuo and the residue was purified by column chromatography eluted with CH2Cl2:MeOH=13:1 to afford the title compound (combined batches yielded 5 g, 43.5% yield over two steps). 1H NMR: (400 MHz, DMSO) δ ppm 11.21 (s, 1H), 10.28 (s, 1H), 8.44 (s, 1H), 7.88 (s, 1H), 7.50 (s, 1H), 6.67-6.68 (m, 1H), 6.22-6.24 (m, 1H), 3.79 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040547B2
Source datasetuspto-grants-2015_05
ORD IDord-4e7e1aa9ed3649d0877c66400808b71c
Source noteuspto-grants-2015_05