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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2358180Generated: November 2, 2026

Chlorosuccinimide → HCID 178431913, compound

https://huagongshe.com/reaction/2358180

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
ReactantHCID 178431887HCID 178431887—
SolventAcetic AcidHCID 176—
ProductHCID 178431913HCID 17843191347.9%

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 numberUS07763643B2
Source datasetuspto-grants-2010_07
ORD IDord-9e5b41ffcbf942a8977f3894434a5836
Source noteuspto-grants-2010_07