HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 625692Generated: October 30, 2026
Triphenylphosphine → (1S,2S)-2-(4-{(R)-7-Fluoro-4-[4-(2-morpholin-4-yl-ethoxy)-phenoxy]-indan-1-yloxy}-phenyl)-cyclopropanecarboxylic acid ethyl ester
https://huagongshe.com/reaction/625692
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2-Morpholinoethanol | HCID 61163 | — |
| Reactant | Di-tert-butyl azodicarboxylate | HCID 97268 | — |
| Reactant | (1S,2S)-2-{4-[(R)-7-Fluoro-4-(4-hydroxy-phenoxy)-indan-1-yloxy]-phenyl}-cyclopropanecarboxylic acid ethyl ester | HCID 118093735 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (1S,2S)-2-(4-{(R)-7-Fluoro-4-[4-(2-morpholin-4-yl-ethoxy)-phenoxy]-indan-1-yloxy}-phenyl)-cyclopropanecarboxylic acid ethyl ester | HCID 118093751 | — |
Reaction Steps
(1S,2S)-2-{4-[(R)-7-Fluoro-4-(4-hydroxy-phenoxy)-indan-1-yloxy]-phenyl}-cyclopropanecarboxylic acid ethyl ester (Intermediate 7, 140 mg, 0.29 mmol), N-(2-hydroxyethyl)morpholine (42 mg, 0.32 mmol), and triphenylphosphine (84 mg, 0.32 mmol) are suspended in dry tetrahydrofuran (5 mL) and cooled to 0° C. Di-tert-butyl azodicarboxylate (74 mg, 0.32 mmol) is added, the mixture is stirred for 2 hours at 0° C. then 2 h at room temperature. The solvent is removed under vacuum and residue is purified by flash chromatography (0-20% ethyl acetate in cyclohexane) to give the title compound. (Yield 175 mg, 55% content). LC (METHOD 6): tR=0.57 min; Mass spectrum (ES+): m/z=562 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09308194B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-9b8d4a1bd48c4d91a50deba0434b3e3d |
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| Source note | uspto-grants-2016_04 |
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