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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1856896Generated: November 1, 2026

Methanol → HCID 18727269, compound

https://huagongshe.com/reaction/1856896

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantTrimethylsilyl iodideHCID 85247—
ReactantHCID 18727270HCID 18727270—
SolventAcetonitrileHCID 6342—
ProductHCID 18727269HCID 1872726943.5%

Reaction Steps

Trimethylsilyl iodide (0.026 ml, 0.19 mmol) was added to a solution of N-hydroxy-6-(benzyloxycarbonyl)amino-2-(R)-{[4-(4-chlorophenyl)piperazine-1-sulfonyl]amino}hexanoamide (103 mg, 0.19 mmol) [prepared as described in Example 17, Step 3] in acetonitrile (2 ml) at 0° C. The reaction mixture was allowed to warm to RT, and additional trimethylsilyl iodide (0.47 mmol, 0.065 ml) was added in 0.5 equiv. portions over 2.5 h. Methanol (1.0 ml) was added and the reaction mixture was concentrated in vacuo. The residue was chromatographed (SiO2, 2%-10% methanol/methylene chloride) to give N-hydroxy-6-amino-2-(R)-{[4-(4-chlorophenyl)piperazine-1-sulfonyl]amino}hexanoamide (43.5%) as a tan solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06143744
Source datasetuspto-grants-2000_11
ORD IDord-442e7cbcfd464dffb8f55169a75dfa8d
Source noteuspto-grants-2000_11