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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1724679Generated: November 2, 2026

Chlorosuccinimide → HCID 68456680, compound

https://huagongshe.com/reaction/1724679

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
ReactantHCID 178431887HCID 178431887—
SolventAcetic AcidHCID 176—
ProductHCID 68456680HCID 68456680103.8%

Reaction Steps

N-(1,4-Dioxaspiro[4.5]dec-6-yl)-N′-(4-methylthiophen-3-yl)guanidine (49 mg) was dissolved in glacial acetic acid (3 ml), and a solution of N-chlorosuccinimide (20.3 mg) in glacial acetic acid (5 ml) was added slowly. The mixture was stirred for a number of hours and then allowed to stand at room temperature over the weekend, after which the glacial acetic acid was removed under reduced pressure, the residue was taken up in water and the mixture was adjusted to pH 10 using 2N sodium hydroxide solution. The basic phase was extracted three times with ethyl acetate and the combined organic phases were dried over magnesium sulfate, filtered and concentrated. The residue was purified by preparative chromatography and the product-containing fractions were combined, freed from acetonitrile, made basic and extracted three times with ethyl acetate. The organic phases were combined, dried (MgSO4) and filtered. Removal of the solvent under reduced pressure gave 24 mg of the desired product which was used directly for the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07488746B2
Source datasetuspto-grants-2009_02
ORD IDord-a08f61f5bfa14d0285e2f49343bcf37d
Source noteuspto-grants-2009_02