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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | [6-(6-Morpholin-4-yl-4-oxo-4H-pyran-2-yl)-thianthren-2-yl]-carbamic acid tert-butyl ester | HCID 59797439 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(7-Amino-thianthren-1-yl)-6-morpholin-4-yl-pyran-4-one | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07429660B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-0da2507423fd4bbe88c839ce057f60ce |
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| Source note | uspto-grants-2008_09 |
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