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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1531157Generated: November 1, 2026

Azidotrimethylsilane → HCID 178433256, compound

https://huagongshe.com/reaction/1531157

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzidotrimethylsilaneHCID 78378—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 178433250HCID 178433250—
SolventTetrahydrofuran ethanolHCID 21873804—
ProductHCID 178433256HCID 178433256—

Reaction Steps

(Z)-1,3-Dihydro-4-fluoro-3-[(4-methyl-1H-imidazol-5-yl)methylene]-5-nitro-2H-indol-2-one (576 mg, 2.0 mmol) (from Example 42 above) was suspended in THF/EtOH (15 mL/8 mL). Hunig's base (diisopropylethyl amine, 5 mL, 30 mmol) (Aldrich) and trimethylsilyl azide (2.6 mL, 20 mmol) (Aldrich) were successively added at r.t. The mixture was heated at reflux for 3 h 20 min. The heterogeneous reaction mixture was cooled to r.t. and the orange suspension was collected by suction filtration. The precipitate was washed with ethanol and dried in a vacuum oven overnight. (Yield 490 mg, 79%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06197804B1
Source datasetuspto-grants-2001_03
ORD IDord-701f295020e24c3aa96aefd2c52dd862
Source noteuspto-grants-2001_03