HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 33799Generated: October 28, 2026
Water → [4-(6-Morpholin-4-yl-4-oxo-4H-pyran-2-yl)-thianthren-1-yloxy]-acetic acid methyl ester
https://huagongshe.com/reaction/33799
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl bromoacetate | HCID 60984 | — |
| Reactant | 2-(4-Hydroxy-thianthren-1-yl)-6-morpholin-4-yl-pyran-4-one | HCID 59797435 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | [4-(6-Morpholin-4-yl-4-oxo-4H-pyran-2-yl)-thianthren-1-yloxy]-acetic acid methyl ester | HCID 59797432 | — |
Reaction Steps
To a solution of 2-(4-Hydroxy-thianthren-1-yl)-6-morpholin-4-yl-pyran-4-one (130) (1.20 g, 2.91 mmol) in dimethylformamide (10 ml), under and inert atmosphere, was added powdered potassium carbonate (1.21 g, 8.75 mmol) and methylbromoacetate (0.55 ml, 5.82 mmol). The temperature of the reaction was raised to 60° C. for 48 hours and then cooled to room temperature before the addition of water (20 mL). The mixture was then extracted using ethyl acetate (3×30 ml). The combined organics were dried (MgSO4), filtered and concentrated in vacuo to give the title compound as an off white solid (1.40 g, 99%) that was suitably clan and required no further purification. m/z (LC-MS, ESP): RT=4.48 min, (M++1)=484
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-a98757de6faa4031934c2f85cda29302 |
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| Source note | uspto-grants-2008_09 |
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