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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2283476Generated: October 31, 2026

Sodium Iodide → Benzyl (2'-((4-isopropyl-3-methylphenyl)carbamoyl)-6-oxo-1,6-dihydro-[3,4'-bipyridin]-5-yl)carbamate

https://huagongshe.com/reaction/2283476

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantBenzyl (2'-((4-isopropyl-3-methylphenyl)carbamoyl)-6-methoxy-[3,4'-bipyridin]-5-yl)carbamateHCID 118261435—
SolventAcetonitrileHCID 6342—
ProductBenzyl (2'-((4-isopropyl-3-methylphenyl)carbamoyl)-6-oxo-1,6-dihydro-[3,4'-bipyridin]-5-yl)carbamateHCID 118261436100.7%

Reaction Steps

To a solution of benzyl (2′-((4-isopropyl-3-methylphenyl)carbamoyl)-6-methoxy-[3,4′-bipyridin]-5-yl)carbamate (216 mg, 0.42 mmol) in MeCN (50 mL) was added trimethylsilylchloride (0.18 mL, 2.1 mmol), sodium iodide (317 mg, 2.10 mmol), and the mixture was stirred at RT for 1.5 h. The precipitate was then collected by filtration. This solid was dissolved in a mixture of MeCN (1 mL) and water (50 mL) and then added to a solution of saturated aq. NaHCO3 (10 mL). The suspension was then stirred for 30 min, filtered and dried to afford benzyl (2′-((4-isopropyl-3-methylphenyl)carbamoyl)-6-oxo-1,6-dihydro-[3,4′-bipyridin]-5-yl)carbamate (210 mg, 99% yield) as a yellow solid: MS (ES) m/z 497 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145393B2
Source datasetuspto-grants-2015_09
ORD IDord-a5210e56c0ce49cf8f18de689d3abe8d
Source noteuspto-grants-2015_09