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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2381788Generated: November 3, 2026

Iodine → HCID 68494041, compound

https://huagongshe.com/reaction/2381788

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantN-benzyl-4-methylthiazole-5-carboxamideHCID 45823040—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68494041HCID 6849404147.1%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of lithium hexamethyldisilazide (4.63 g, 27.65 mmol) in anhydrous tetrahydrofuran (25 mL) was added dropwise to a solution of N-benzyl-4-methylthiazole-5-carboxamide (2.79 g, 12.02 mmol) in anhydrous tetrahydrofuran (25 mL) at −78° C. under nitrogen atmosphere. The reaction mixture was stirred at −78° C. for 1 hour, then iodine (1.68 g, 13.22 mmol) was added in portions. The mixture was stirred at ambient temperature for 90 minutes, quenched with methanol (2 mL) and water (2 mL). The solvent was removed in vacuo and the residue was diluted with water (30 mL) and extracted with dichloromethane (3×40 mL). The organic layers were combined, dried over anhydrous sodium sulphate, filtered and concentrated in vacuo. The residue was purified by column chromatography (20-35% ethyl acetate in hexanes) to afford the title compound as a white solid (2.03 g, 47%): 1H NMR (300 MHz, CDCl3) δ 7.39-7.30 (m, 5H), 6.02 (br s, 1H), 4.57 (d, J=6.0 Hz, 2H), 2.68 (s, 3H); MS (ES+) m/z 359.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258160B2
Source datasetuspto-grants-2012_09
ORD IDord-48d5dc46a7e8446199d8c7cc4900d598
Source noteuspto-grants-2012_09