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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1505994Generated: November 1, 2026

2,2,2-Trifluoroethyl trifluoromethanesulfonate → HCID 67027535, compound

https://huagongshe.com/reaction/1505994

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2,2-Trifluoroethyl trifluoromethanesulfonateHCID 80366—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 67203172HCID 67203172—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67027535HCID 6702753585%

Reaction Steps

N,N-Diisopropylethylamine (100 mg, 0.77 mmol) and trifluoromethane sulfonic acid 2,2,2-trifluoroethyl ester (100 mg, 0.43 mmol) in THF (1 mL) were added to a solution of 9-benzenesulfonyl-5-piperidin-4-ylmethyl-9H-dipyrido[2,3-b;4′,3′-d]pyrrole-6-carbonitrile in THF (4 mL) and resultant mixture stirred at ambient temperature for 30 min. The mixture was then filtered through a 2 g Sill SPE cartridge, eluting with THF. The THF washings were concentrated in vacuo and the resultant residue was purified by flash chromatography (silica, 2 g column, Si H SPE, 0-20% ethyl acetate in DCM) to afford title compound as a white solid (0.16 g, 85%). 1H NMR (CDCl3, 400 MHz): 9.81 (d, J=2.9 Hz, 1H), 8.81-8.75 (m, 1H), 8.34 (d, J=8.1 Hz, 1H), 8.28 (d, J=7.9 Hz, 2H), 7.66-7.59 (m, 1H), 7.55-7.45 (m, 3H), 3.35-3.27 (m, 2H), 3.02-2.88 (m, 5H), 2.32-2.21 (m, 2H), 1.86-1.60 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216980B2
Source datasetuspto-grants-2015_12
ORD IDord-3edd78a98c36488a9456fb03a3a5a995
Source noteuspto-grants-2015_12