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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1264632Generated: October 31, 2026

2-Cyano-3,3-bis(methylthio)acrylamide → 2-Cyano-3-[[(3S)-hexahydro-2-oxo-1-(phenylmethyl)-1H-azepin-3-yl]amino]-3-[(2-methyl-5-benzofuranyl)amino]-propenamide

https://huagongshe.com/reaction/1264632

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Cyano-3,3-bis(methylthio)acrylamideHCID 2747746—
Reactant2-Methyl-5-benzofuranamineHCID 3157484—
Reactant3-Amino-1-benzyl-azepan-2-oneHCID 18612599—
SolventEthanolHCID 702—
Product2-Cyano-3-[[(3S)-hexahydro-2-oxo-1-(phenylmethyl)-1H-azepin-3-yl]amino]-3-[(2-methyl-5-benzofuranyl)amino]-propenamideHCID 7003203637%

Reaction Steps

Preparation of title compound. A solution of 2-methyl-5-benzofuranamine (32 mg, 0.22 mmol) and 3,3-bis(methylthio)-2-cyanoacrylamide (41 mg, 0.22 mmol) in ethanol (0.35 mL) was stirred at 80° C. After stirring for 5 h, a solution of 3-aminohexahydro-1-phenylmethyl-2H-azepin-2-one (74 mg, 0.29 mmol) in ethanol (0.74 mL) was added. After stirring at 80° C. for 2 days, the reaction was purified by column chromatography (silica, 1% methanol/dichloromethane) to afford the title compound (37 mg, 37% yield): MS (ESI, pos. ion spectrum) m/z 458; HPLC (method A) tR 4.13 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06544981B2
Source datasetuspto-grants-2003_04
ORD IDord-44dae7d193bc481b8840d58d8d9c28f4
Source noteuspto-grants-2003_04