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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1242042Generated: November 1, 2026

2-(Ethoxymethylene)propanedinitrile → N-(1,3-Benzothiazol-5-yl)acetamide

https://huagongshe.com/reaction/1242042

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Ethoxymethylene)propanedinitrileHCID 67152—
ReactantN-(3-Amino-4-sulfanylphenyl)acetamideHCID 21937579—
SolventAcetic AcidHCID 176—
ProductN-(1,3-Benzothiazol-5-yl)acetamideHCID 28520517%

Reaction Conditions

Temperature125 °C

Reaction Steps

To a solution of intermediate 3′-amino-4′-mercaptoacetanilide in HOAc (50 mL) was added ethoxymethylene malononitrile (1.95 g, 16 mmol) and the resulting mixture was refluxed at 125° C. for 5 h. After cooling, the product mixture was concentrated under reduced pressure, and the residue was partitioned between saturated aqueous NaHCO3 and EtOAc. The aqueous phase was extracted with EtOAc, and the combined extracts were washed with brine, dried over Na2SO4 and concentrated. The residue was purified by chromatography on silica gel, eluting with EtOAc-Hex (0:100 to 50:50) to give the title compound (508 mg, 17%) as a yellow solid. 1H-NMR (DMSO-d6): δ 9.35 (1H, s), 8.53 (1H, s), 8.10 (1H, d), 7.63 (1H, d), 2.15 (3H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115640B2
Source datasetuspto-grants-2006_10
ORD IDord-0e77c3d872a748bd842f90cd03aab956
Source noteuspto-grants-2006_10