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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 33793Generated: October 27, 2026

Trifluoroacetic acid → 2-(7-Amino-thianthren-1-yl)-6-morpholin-4-yl-pyran-4-one

https://huagongshe.com/reaction/33793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant[6-(6-Morpholin-4-yl-4-oxo-4H-pyran-2-yl)-thianthren-2-yl]-carbamic acid tert-butyl esterHCID 59797439—
SolventDichloromethaneHCID 6344—
Product2-(7-Amino-thianthren-1-yl)-6-morpholin-4-yl-pyran-4-oneHCID 59797427—

Reaction Steps

To a solution of [6-(6-morpholin-4-yl-4-oxo-4H-pyran-2-yl)-thianthren-2-yl]-carbamic acid tert-butyl ester (11.95 g, 23.4 mmol) in dichloromethane (150 ml) was added trifluoroacetic acid (30 ml) and left under stirring at room temperature overnight. The solvent was dried in vacuo revealing a viscous dark brown liquid. Saturated sodium bicarbonate solution (400 ml) was added to the residue, which was left to stir for 20 minutes. The brown precipitate was filtered, washing with water and left to dry in a vacuum desiccator overnight. The solid was then purified by column chromatography (silica, MeOH/Dichloromethane, 3:97, Rf=0.28). 1HNMR (300 MHz, CDCl3): δH=3.24 (2H, bs); 3.46 (4H, bs); 3.81 (4H, bs); 6.33 (1H, s); 6.58 (1H, m); 6.86 (1H, d); 7.21 (1H, d); 7.30 (1H, t); 7.38 (1H, d); 7.63 (1H, d); m/z (LC-MS, ESP), RT=3.8 min, (M++1)=411

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07429660B2
Source datasetuspto-grants-2008_09
ORD IDord-0da2507423fd4bbe88c839ce057f60ce
Source noteuspto-grants-2008_09