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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1264633Generated: October 26, 2026

Dimethyl malonate → [[[(3S)-Hexahydro-2-oxo-1-[2-oxo-2-(1-pyrrolidinyl)ethyl]-1H-azepin-3-yl]amino][(2-methyl-5-benzofuranyl)amino]methylene]propanedioic acid dimethyl ester

https://huagongshe.com/reaction/1264633

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl malonateHCID 7943—
ReactantSodium hydrideHCID 24758—
Reactant5-Isothiocyanato-2-methylbenzofuranHCID 12047819—
Reactant(S)-1-[(3-amino-hexahydro-2-oxo-1H-azepin-1-yl)acetyl]pyrrolidineHCID 12047820—
CatalystMercuric ChlorideHCID 24085—
SolventDimethylformamideHCID 6228—
Product[[[(3S)-Hexahydro-2-oxo-1-[2-oxo-2-(1-pyrrolidinyl)ethyl]-1H-azepin-3-yl]amino][(2-methyl-5-benzofuranyl)amino]methylene]propanedioic acid dimethyl esterHCID 7003084240%

Reaction Steps

Sodium hydride (95%, 11 mg, 0.44 mmol) was added to a solution of dimethyl malonate (40 mg, 0.30 mmol) in DMF (1.5 mL) at 0° C. The resulting mixture was warmed to room temperature, 2-methyl-5-isothiocyanatobenzofuran (56 mg, 0.30 mmol) was then added, and the resulting solution was stirred at at room temperature for 30 minutes. To the solution was then added 1-[[(3S)-3-aminohexahydro-2-oxo-1H-azepin-1-yl]acetyl]pyrrolidine (71 mg, 0.30 mmol) followed by mercury (II) chloride (82 mg, 0.30 mmol). The resulting dark mixture was stirred at room temperature for 2 h, then filtered through CELITE. The filtrate was concentrated, and the residue was purified by flash chromatography (silica, 1 to 5% methanol/dichloromethane) to afford the title compound as a pale yellow solid (63 mg, 40%): MS (ESI, pos. ion spectrum) m/z 527, HPLC (method A): tR 3.5 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06544981B2
Source datasetuspto-grants-2003_04
ORD IDord-72c666fe3752479fae806bb1a6491453
Source noteuspto-grants-2003_04