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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725176Generated: November 2, 2026

Guanidine Hydrochloride → HCID 178513101, compound

https://huagongshe.com/reaction/1725176

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGuanidine HydrochlorideHCID 5742—
ReactantSodium ethoxideHCID 2723922—
ReactantHCID 86607187HCID 86607187—
SolventMethanolHCID 887—
ProductHCID 178513101HCID 17851310157%

Reaction Steps

To a solution of guanidine hydrochloride in anhydrous MeOH (1.5 ml) was added powder NaOEt (80 mg. 1.17 mmol). After 10 min stirring at room temperature, the reaction mixture was treated with tert-butyl [2-(2-furylmethyl)-5-phenyl-1H-pyrrol-1-yl]acetate. After 5 h stirring at 55° C., the reaction mixture was cooled and quenched with H2O (5 ml), diluted with EtOAc (15 ml). The organic layer was separated and the aqueous was extracted with EtOAc (2×15 ml). The combined organic extracts were washed with H2O (15 ml), brine (15 ml), dried (Na2SO4) and concentrated. The crude material was purified by chromatography (silica gel; EtOAc/2M NH3 in MeOH: 97/3) to give the titled compound (73 mg, 57%) as a solid: mp 80-82° C.; MS (−) ES, 321 (M−H)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07488832B2
Source datasetuspto-grants-2009_02
ORD IDord-1717e5acb8024c68ad19993ae06c43f9
Source noteuspto-grants-2009_02