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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1641094Generated: November 2, 2026

Trifluoromethanesulfonic anhydride → HCID 59418739, compound

https://huagongshe.com/reaction/1641094

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantHCID 59418696HCID 59418696—
SolventDichloromethaneHCID 6344—
ProductHCID 59418739HCID 59418739—

Reaction Conditions

Temperature0 °C

Reaction Steps

Trifluoromethanesulfonic anhydride (1.93 g, 6.86 mmol) was added dropwise to tert-butyl 7-(5-hydroxy-6-(methoxycarbonyl)pyridin-2-yl)-3,4-dihydroquinoline-1(2H)-carboxylate (29D) (2.40 g, 6.23 mmol) and TEA (0.95 g, 9.35 mmol) in anhydrous DCM (25 mL) at 0° C. The reaction mixture was stirred at 0° C. for 1.5 hours, diluted with DCM, washed with 10% citric acid, dried over MgSO4, filtered, and concentrated under reduced pressure. The crude material was purified by column chromatography on silica gel eluting with a gradient of PE:EtOAc 88:12-82:18 to provide tert-butyl 7-(6-(methoxycarbonyl)-5-(trifluoromethylsulfonyloxy)pyridin-2-yl)-3,4-dihydroquinoline-1(2H)-carboxylate (29E): 1H NMR (300 MHz, CDCl3) δ 8.40 (1H d), 7.95 (1H, d), 7.71 (1H, d), 7.66 (1H, dd), 7.19 (1H, d), 4.04 (3H, s), 3.75 (2H, m), 2.82 (2H, t), 1.96 (2H, m), 1.56 (9H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08114893B2
Source datasetuspto-grants-2012_02
ORD IDord-da72dd79a2104e12acfadf2a745f27f0
Source noteuspto-grants-2012_02