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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1070894Generated: November 1, 2026

Sodium Iodide → HCID 10152457, compound

https://huagongshe.com/reaction/1070894

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantDimethylformamideHCID 6228—
ReactantTriethylamineHCID 8471—
Reactant2-chloro-N,N-dimethylacetamideHCID 75886—
ReactantMiridesapHCID 125516—
ProductHCID 10152457HCID 1015245784%

Reaction Conditions

Temperature100 °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 103 ml (1 mmol) 2-chloro-N,N-dimethylacetamide in 2.5 ml dimethylformamide were added 14.9 mg (0.1 mmol) sodium iodide and 139 ml (1 mmol) triethylamine. After stirring overnight at 100° C. the solvent was distilled off, the residue was taken up with dichloromethane and extracted with water. The organic extracts were dried with sodium sulfite and the solvent was distilled off to yield 190 mg (84%) of (R)-1-{6-[(R)-2-(dimethylcarbamoyl-methoxycarbonyl)-pyrrolidin-1-yl]-6-oxo-hexanoyl}-pyrrolidine-2-carboxylic acid dimethylcarbamoyl-methyl ester as a yellow oil, MS m/e (%): 511 (M+H+, 100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06903129B2
Source datasetuspto-grants-2005_06
ORD IDord-084f65d3401b45229f8ab3ac8fdc2848
Source noteuspto-grants-2005_06