Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2117756Generated: October 31, 2026

Guanidine Hydrochloride → HCID 178494668, compound

https://huagongshe.com/reaction/2117756

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGuanidine HydrochlorideHCID 5742—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 178494669HCID 178494669—
Solvent1-ButanolHCID 263—
ProductHCID 178494668HCID 17849466860.4%

Reaction Steps

5-(3-Dimethylaminoprop-2-en-1-oyl)-1-methoxyisopropyl-2-methoxymethylimidazole (Method 56; 3.13, 11.1 mmol) and guanidine hydrochloride (2.65 g, 27.8 mmol) were suspended in 1-butanol (20 ml). Sodium methoxide (2.4 g, 44 mmol) was added in one portion and the mixture heated under reflux, under an atmosphere of nitrogen, for 18 hours. The volatiles were removed by evaporation. Water (50 ml) was added and extracted EtOAc (3×50 ml). The organic layers were combined and dried with Chemelut CE1010 and the solvent evaporated in vacuo. The residue was purified by flash silica chromatography eluting with DCM:MeOH (100:0 increasing in polarity to 95:5) to give the title compound as an orange solid (1.86 g, 60%). NMR: 1.43 (d, 3H), 3.16 (s, 3H), 3.24 (s, 3H), 3.63 (m, 1H), 3.89 (m, 1H), 4.50 (q, 2H), 5.26 (m, 1H), 6.57 (s, 2H), 6.80 (d, 1H), 7.40 (s, 1H), 8.21 (d, 1H); m/z 278.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07442697B2
Source datasetuspto-grants-2008_10
ORD IDord-9b93e17b15db496cb04b2e827237c41c
Source noteuspto-grants-2008_10