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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1908297Generated: October 28, 2026

1,1,1-Trifluoro-N-phenylmethanesulfonamide → 2-[(3-Hydroxy-5-trifluoromethanesulfonyloxy-pyridine-2-carbonyl)-amino]-2-methyl-propionic acid methyl ester

https://huagongshe.com/reaction/1908297

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1,1-Trifluoro-N-phenylmethanesulfonamideHCID 68012—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-[(3,5-Dihydroxy-pyridine-2-carbonyl)-amino]-2-methyl-propionic acid methyl esterHCID 59513081—
SolventMethanolHCID 887—
Product2-[(3-Hydroxy-5-trifluoromethanesulfonyloxy-pyridine-2-carbonyl)-amino]-2-methyl-propionic acid methyl esterHCID 5951307836%

Reaction Steps

To a solution in 2-[(3,5-dihydroxy-pyridine-2-carbonyl)-amino]-2-methyl-propionic acid methyl ester, 18, (0.312 g, 1.23 mmol) in MeOH (10 mL) containing diisopropylethylamine (0.214 mL, 1.23 mmol) at 0° C. under N2 is added N-phenyltrifluoromethanesulfonamide (0.439 g, 1.23 mmol). The reaction is warmed slowly to room temperature and stirred for 40 hours. The solvent is removed under reduced pressure and the crude oil which remains is purified over silica (EtOAc:heptane 1:9) to afford 0.170 g (36% yield) of the desired compound as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598210B2
Source datasetuspto-grants-2013_12
ORD IDord-ac81b01b0a364a8c9bdd027223a26cd9
Source noteuspto-grants-2013_12