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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 914837Generated: October 31, 2026

Water → N-methoxy-N-methyl-1-(tert-butoxycarbonyl)-4-fluoropiperidine-4-carboxamide

https://huagongshe.com/reaction/914837

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
Reactant1-(tert-Butoxycarbonyl)-4-fluoropiperidine-4-carboxylic AcidHCID 21050397—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductN-methoxy-N-methyl-1-(tert-butoxycarbonyl)-4-fluoropiperidine-4-carboxamideHCID 2224858290.6%

Reaction Steps

After dissolving 2.19 g of 1-(tert-butoxycarbonyl)-4-fluoropiperidine-4-carboxylic acid in 30 ml of dichloromethane, 2.16 g of 1,1′-carbonyldiimidazole was added and the mixture was stirred at room temperature for 1.5 hours. Next, 1.30 g of N-methyl-O-methylhydroxylamine hydrochloride was added and the mixture was stirred overnight at room temperature. Water was added to the reaction solution, and extraction was performed with ethyl acetate. The organic layer was washed with aqueous sodium carbonate solution, water and saturated brine in that order and dried over anhydrous magnesium sulfate, and then the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (solvent: n-hexane/ethyl acetate) to obtain the title compound (2.33 g, 90% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07265108B2
Source datasetuspto-grants-2007_09
ORD IDord-5c3fc2365fba4508a32c48f2c8562cde
Source noteuspto-grants-2007_09