Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2421847Generated: November 2, 2026

Sodium Iodide → HCID 57617824, compound

https://huagongshe.com/reaction/2421847

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantMethyl 3-amino-4-(4-chloro-2-methylbutan-2-ylthio)benzoateHCID 67242880—
SolventMethyl Ethyl KetoneHCID 6569—
ProductHCID 57617824HCID 5761782467%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of methyl 3-amino-4-(4-chloro-2-methylbutan-2-ylthio)benzoate (3.11 g, 10.8 mmol) in 2-butanone (150 mL) was added sodium iodide (4.86 g, 32.4 mmol). The reaction was heated to 70° C. and stirred at that temperature for 16 hours. Thin layer chromatography and LCMS analysis of the reaction mixture indicated consumption of starting material. The solvent was removed under reduced pressure and the resulting red slurry was diluted with EtOAc (200 mL). The organic layer was washed with saturated aqueous NaHCO3 (100 mL) and aqueous sodium hydrosulifte (50 mL). The organic layer was dried over Na2SO4 and concentrated in vacuo. The resulting solid was purified by flash column chromatography using a gradient elution of hexanes with 5-70% EtOAc to provide methyl 2,2-dimethyl-2,3,4,5-tetrahydrobenzo-[b][1,4]thiazepine-7-carboxylate (1.82 g, 7.24 mmol, 67.0% yield) as an off white solid. LCMS (+ESI) m/z=252.1 [M+H]+; 1H-NMR (CDCl3) δ 7.48-7.40 (m, 3H), 4.25-4.06 (br s, 1H), 3.88 (s, 3H), 3.25 (m, 2H), 2.00 (m, 2H), 1.33 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960376B2
Source datasetuspto-grants-2011_06
ORD IDord-2b288d214b2e47de8f6d1acb918dec82
Source noteuspto-grants-2011_06