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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1736349Generated: November 2, 2026

Hydrochloric Acid → HCID 178464594, compound

https://huagongshe.com/reaction/1736349

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIsopropanolHCID 3776—
ReactantHCID 178464582HCID 178464582—
SolventMethanolHCID 887—
ProductHCID 178464594HCID 178464594—

Reaction Steps

A mixture of 3.1 g (±)-N"-cyano-N-[3-[[(3,4-dihydro-2H-1-benzopyran-2-yl)methyl]amino]propyl]-N'-ethylguanidine in a solution of 10 ml hydrochloric acid in 2-propanol and 50 ml methanol was stirred and refluxed for 30 minutes. The solvent was evaporated. The residue was dissolved in water and this mixture was alkalized with aqueous NaOH (10% ). This mixture was extracted with CH2Cl2. The organic layer was separated, washed with water, dried (MgSO4), filtered and the solvent was evaporated. The residue was purified by column chromatography over silica gel (eluent: CH2Cl2 /CH3OH/(NH3) 90:10). The pure fractions were collected and the solvent was evaporated. The residue was dissolved in 2-propanol and converted into the hydrochloric acid salt (1:2) with 2-propanol saturated with HCl. The salt was filtered off and recrystallized from 2-propanol. The crystals were filtered off and dried, yielding 2.95 g (±)-N-[[[3-[[(3,4-dihydro-2H-1-benzopyran-2-yl)methyl]amino]propyl]amino](ethylamino)methylene]urea dihydrochloride; mp. 182.2° C. (interm. 51).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05541180
Source datasetuspto-grants-1996_07
ORD IDord-7781a71c12c54045b3ae460d359955b0
Source noteuspto-grants-1996_07