Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444755Generated: November 2, 2026

Hydrochloric Acid → HCID 67336959, compound

https://huagongshe.com/reaction/1444755

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl 3-(5-formylfuran-2-yl)thiophene-2-carboxylateHCID 2797068—
Reactant3-(5-Ammoniopentanoyl)pyridinium chlorideHCID 67337657—
SolventIsopropanolHCID 3776—
ProductHCID 67336959HCID 6733695997.7%

Reaction Conditions

Temperature80 °C

Reaction Steps

3-(5-Ammoniopentanoyl)pyridinium chloride (99 mg, 0.39 mmol) and methyl 3-(5-formyl-2-furyl)thiophene-2-carboxylate (102 mg, 0.43 mmol) were combined in a reaction vessel and treated with isopropanol (6 mL). The reaction vessel was sealed and the reaction was heated to 80° C. with stirring overnight. The reaction was cooled to room temperature. The precipitate was recovered by vacuum filtration, then treated with saturated NaHCO3(aq) and extracted three times with EtOAc. The EtOAc extracts were washed with brine, combined, dried over Na2SO4, filtered, concentrated under reduced pressure, and eluted through a 20 gram column of silica gel with 99:1:0.1 CH2Cl2:MeOH:NH4OH (1 liter). The recovered material was dissolved into MeOH and treated with 2 eq. of 6 N HCl(aq). This solution was concentrated under reduced pressure and the recovered material was dissolved into hot isopropanol to re-crystallize. Crystals were recovered by vacuum filtration, washed with a 20 isopropanol in hexane solution, and then with ether, then dried under vacuum giving 86 mg (48%) of an orange solid. LC-MS: RT=5.25 min, [M+H]+=379.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662965B2
Source datasetuspto-grants-2010_02
ORD IDord-9524916aa24c4ae69863c4ea940ec865
Source noteuspto-grants-2010_02