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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1070895Generated: October 30, 2026

Sodium Iodide → HCID 10175121, compound

https://huagongshe.com/reaction/1070895

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantDimethylformamideHCID 6228—
ReactantTriethylamineHCID 8471—
ReactantChloro-N,N-diethylacetamideHCID 16844—
ReactantMiridesapHCID 125516—
ProductHCID 10175121HCID 1017512192%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of 170 mg (0.5 mmol) (R)-1-[6-[(R)-2-carboxy-pyrrolidin-1-yl]-6-oxo-hexanoyl]-pyrrolidine-2-carboxylic acid and 137 ml (1 mmol) 2-chloro-N,N-diethylacetamide in 3 ml dimethylformamide were added 14.9 mg (0.1 mmol) sodium iodide and 139 ml (1 mmol) triethylamine. After stirring overnight at 90° C. the solvent was distilled off, the residue was taken up with dichloromethane and extracted with water. The organic extracts were dried with sodium sulfate and the solvent was distilled off to yield 260 mg (92%) of (R)-1-{6-[(R)-2-(diethylcarbamoyl-methoxycarbonyl)-pyrrolidin-1-yl]-6-oxo-hexanoyl}-pyrrolidine-2-carboxylic acid diethylcarbamoyl-methyl ester as a yellow oil, MS m/e (%): 567 (M+H+, 100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06903129B2
Source datasetuspto-grants-2005_06
ORD IDord-3cd242875e324798acfaa863b852dedf
Source noteuspto-grants-2005_06