HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 394323Generated: October 30, 2026
Triphenylphosphine → HCID 68616363, compound
https://huagongshe.com/reaction/394323
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | 4-Chlorothiobenzamide | HCID 2734826 | — |
| Reactant | Methyl 4-bromo-3-oxopentanoate | HCID 9815681 | — |
| Reactant | 2-[2-(4-Chloro-phenyl)-5-methyl-thiazol-4-yl]-ethanol | HCID 22647624 | — |
| Reactant | Ethyl 3-(3,5-difluoro-4-hydroxyphenyl)-2-ethoxypropanoate | HCID 59419836 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68616363 | HCID 68616363 | — |
Reaction Steps
In analogy to the procedure described in example 4 d], [rac]-3-(3,5-difluoro-4-hydroxy-phenyl)-2-ethoxy-propionic acid ethyl ester [example 70 a]] was reacted with 2-[2-(4-chloro-phenyl)-5-methyl-thiazol-4-yl]-ethanol (prepared from [rac]-4-bromo-3-oxo-pentanoic acid methyl ester [PCT Int. Appl. (2001), WO 01/79202] and 4-chloro-thiobenzamide in analogy to the procedures described in examples 12 a] and 12 b]) in tetrahydrofuran in the presence of triphenylphosphine and DEAD (diethyl azodicarboxylate) to yield [rac]-3-(4-{2-[2-(4-chloro-phenyl)-5-methyl-thiazol-4-yl]-ethoxy}-3,5-difluoro-phenyl)-2-ethoxy-propionic acid ethyl ester, which was further saponified in analogy to the procedure described in example 4 e], to yield [rac]-3-(4-{2-[2-(4-chloro-phenyl)-5-methyl-thiazol-4-yl]-ethoxy}-3,5-difluoro-phenyl)-2-ethoxy-propionic acid as light yellow amporphous solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06809110B2 |
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| Source dataset | uspto-grants-2004_10 |
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| ORD ID | ord-3b310d28ff384aa99c99ad113eef190a |
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| Source note | uspto-grants-2004_10 |
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