HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19556Generated: October 26, 2026
Triphenylphosphine → 6-(2-morpholine-4-ylethoxy)-1-oxo-3-pheny-1H-indene-2-carboxylic acid cyclohexylamide
https://huagongshe.com/reaction/19556
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2-Morpholinoethanol | HCID 61163 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | 6-hydroxy-1-oxo-3-phenyl-1H-indene-2-carboxylic acid cyclohexylamide | HCID 68697166 | — |
| Solvent | Tetrahydropyran benzene | HCID 86615313 | — |
| Product | 6-(2-morpholine-4-ylethoxy)-1-oxo-3-pheny-1H-indene-2-carboxylic acid cyclohexylamide | HCID 68698349 | 88.3% |
Reaction Steps
6-Hydroxy-1-oxo-3-phenyl-1H-indene-2-carboxylic acid cyclohexylamide (141 mg, 0.41 mmol) obtained in Step 3 was dissolved in tetrahydropyran/benzene (3 mL/2 mL), and 4-(2-hydroxyethyl)morpholine (99 μl, 0.82 mmol) and triphenylphosphine (215 mg, 0.82 mmol) were added thereto. Then, diisopropyl azodicarboxilate (149 μl, 0.82 mmol) was added slowly thereto at 0° C., and stirred for 2 hrs at RT. The resulting mixture washed with saturated saline and extracted with ethyl acetate. The organic layer was separated, dried over anhydrous MgSO4 and concentrated under a reduced pressure. The resulting residue was purified by flash chromatography to obtain 165 mg of the titled compound (yield: 88.3%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07745439B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-e8d480256d7b46968a7d67c25afe805a |
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| Source note | uspto-grants-2010_06 |
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