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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1281623Generated: November 1, 2026

Acetic Acid → HCID 69985672, compound

https://huagongshe.com/reaction/1281623

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium IodideHCID 5238—
ReactantTrichloromethylsilaneHCID 6399—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant(R)-N-(5-(2-amino-1-hydroxyethyl)-2-hydroxyphenyl)methanesulfonamideHCID 12047933—
ReactantHCID 18173889HCID 18173889—
SolventMethanolHCID 887—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
ProductHCID 69985672HCID 699856729.4%

Reaction Steps

N-[4-(2,2-Dimethoxyethyl)phenyl]-1-(4-phenyl-1,3-thiazol-2-yl)-4-piperidinamine (0.415 g, 30 0.98 mmol) was added to a pre-prepared mixture of sodium iodide (0.367 g, 2.45 mmol) and trichloro(methyl)silane (0.229 mL, 1.95 mmol) in anhydrous acetonitrile (70 mL). The reaction was stirred at ambient temperature for 10 minutes. Dichloromethane was added and the reaction washed with 10% sodium thiosulfate solution, water and brine. The organic layer was dried with anhydrous magnesium sulfate, filtered and the solvent partially removed in vacuo. The aldehyde solution was used directly and treated with methanol, acetic acid (0.088 mL, 1.47 mmol), N-{5-[(1R)-2-amino-1-hydroxyethyl]-2-hydroxyphenyl}methanesulfonamide (0.241 g, 0.98 mmol) followed by sodium cyanoborohydride (0.067 g, 0.97 mmol). The reaction was stirred at ambient temperature overnight. The reaction was taken to dryness in vacuo, adsorbed onto silica and purified by flash chromatography on silica gel Merck-60 (eluant: 5:1 chloroform-methanol containing 1% ammonium hydroxide) to yield the title compound (0.092 mmol, 0.151 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06451814B1
Source datasetuspto-grants-2002_09
ORD IDord-8dc65024c49c4ceda8449d6d773c4d9d
Source noteuspto-grants-2002_09