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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1741720Generated: November 2, 2026

Trimethylsilyl isocyanate → HCID 9803758, compound

https://huagongshe.com/reaction/1741720

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl isocyanateHCID 70696—
ReactantHCID 18963909HCID 18963909—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 9803758HCID 9803758—

Reaction Steps

To a solution of 2-(4'-fluoro-4-biphenylylmethyl)-6-[2-(N-hydroxyamino)ethoxy]-1-oxo-1,2,3,4-tetrahydroisoquinoline (~22.5 mmol) in 1,4-dioxane (50 ml) and methylene chloride (30 ml), is added trimethylsilylisocyanate (3.36 ml). The reaction mixture is stirred at room temperature overnight and is subsequently diluted with H2O (500 ml). The resulting solution is extracted with EtOAc (2×400 ml) and the combined EtOAc portions washed with 2N HCl (800 ml), saturated NaCl solution (800 ml), dried over MgSO4, and concentrated in vacuo. The resulting solid is recrystallized from EtOAc/hexanes to give 2-(4'-fluoro-4-biphenylylmethyl)-6-[2-(N-aminocarbonyl-N-hydroxyamino)-ethoxy]-1-oxo-1,2,3,4-tetrahydroisoquinoline, m.p. 171°-172°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05334600
Source datasetuspto-grants-1994_08
ORD IDord-486a301b1a5548ff918bdedb400cea72
Source noteuspto-grants-1994_08