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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 746621Generated: October 28, 2026

Sodium Iodide → HCID 11624273, compound

https://huagongshe.com/reaction/746621

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantAmmonium HydroxideHCID 14923—
ReactantSodium ThiosulfateHCID 24477—
ReactantHCID 11566634HCID 11566634—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
ProductHCID 11624273HCID 11624273—

Reaction Conditions

Temperature100 °C

Reaction Steps

NaI was taken up in acetonitrile (30 mL) under N2 and trimethylsilyl chloride was slowly added (2.97 mL, 24 mmol). The mixture was stirred for 15 min after which a solution of 1-[2-(2-pyrrolidin-1-yl-ethyl)-benzo[b]thiophen-3-yl]-1-thiazol-4-yl-ethanol (1.4 g, 3.91 mmol) in acetonitrile (30 mL) and dichloromethane (10 mL) was added. The reaction was heated in a closed vessel to 100° C. for 3 hrs. After cooling to room temperature 1M sodium thiosulfate was added followed by NH4OH until pH ˜9. After extraction with EtOAc, drying (MgSO4), filtering, concentration in vacuo and subsequently purification by mass triggered preparative HPLC, 4-{1-[2-(2-pyrrolidin-1-yl-ethyl)-benzo[b]thiophen-3-yl]-vinyl}-thiazole (Compound 19-3) was isolated MH+=341.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07393865B2
Source datasetuspto-grants-2008_07
ORD IDord-888ad8cf5f4d471a860a483a5bc3d605
Source noteuspto-grants-2008_07