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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1070835Generated: October 31, 2026

Pyridine → HCID 22398289, compound

https://huagongshe.com/reaction/1070835

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetyl chlorideHCID 6367—
Reactant3-Methylisothiazol-5-ylamine hydrochlorideHCID 2723918—
ProductHCID 22398289HCID 22398289—

Reaction Steps

Compounds 179 and 189 were synthesized as shown Scheme 7. Reaction of 5-amino-3-methylisothiazole hydrochloride with acetic chloride in pyridine followed by nitration and reduction gave an intermediate of 4-amino-5-acetamido-3-methylisothiazole. Reaction of the intermediate (1.2 eq ) with DBD under N2 afforded Compound179. Refluxing 4-nitro-5-acetamido-3-methylisothiazole in 4N HCl aq. and further reacting with DBD under N2 with refluxing yielded Compound 189.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06903133B2
Source datasetuspto-grants-2005_06
ORD IDord-1472b606c43d42c2972cad841c077d5b
Source noteuspto-grants-2005_06