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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 888262Generated: October 26, 2026

2-Methoxyphenylacetic acid → 2-(2-methoxyphenyl)-N-[2-[2-[[3-(trifluoromethyl)-phenyl]sulfonyl]-ethylsulfanyl]-pyridin-3-yl]acetamide

https://huagongshe.com/reaction/888262

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methoxyphenylacetic acidHCID 7134—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant[2-[2-[[3-(Trifluoromethyl)phenyl]sulfonyl]-ethylsulfanyl]-pyridin-3-yl]amineHCID 67133713—
SolventDichloromethaneHCID 6344—
SolventHexaneHCID 8058—
Product2-(2-methoxyphenyl)-N-[2-[2-[[3-(trifluoromethyl)-phenyl]sulfonyl]-ethylsulfanyl]-pyridin-3-yl]acetamideHCID 4691743481%

Reaction Conditions

Temperature0 °C

Reaction Steps

1.7 g (4.0 mmol) HATU and 1.36 ml (8.0 mmol) DIPEA were added to a solution of 582 mg (3.5 mmol) 2-(2-methoxyphenyl)acetic acid in DCM (10 ml) and the mixture was cooled to 0° C. After stirring for 15 min a solution of 725 mg (2.0 mmol) [2-[2-[[3-(trifluoromethyl)phenyl]sulfonyl]-ethylsulfanyl]-pyridin-3-yl]amine (VPF-001) in DCM (6 ml) was added at 0° C. The mixture was then stirred for 16 h at room temperature. Then it was diluted with DCM and washed successively with a saturated aqueous NH4Cl solution, a saturated aqueous NaHCO3 solution and brine. The organic phase was dried over Na2SO4, filtered and concentrated to small volume under vacuum. Column chromatography (hexane/EE 7:3) of the residue yielded 827 mg (1.6 mmol, 81%) 2-(2-methoxyphenyl)-N-[2-[2-[[3-(trifluoromethyl)-phenyl]sulfonyl]-ethylsulfanyl]-pyridin-3-yl]acetamide. MS: m/z 511.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247573B2
Source datasetuspto-grants-2012_08
ORD IDord-016d65e1ac3c42759c453fa7af7cea95
Source noteuspto-grants-2012_08