HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2277261Generated: October 29, 2026
Trifluoroacetic acid → N-((2S)-1-((2-(4-hydroxyphenyl)[1,3]thiazolo[4,5-c]pyridin-6-yl)oxy)propan-2-yl)acetamide
https://huagongshe.com/reaction/2277261
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | 2-ethylhexyl 3-((2-(((2S)-2-acetamidopropyl)oxy)-5-((4-(cyclopropylmethoxy)benzoyl)amino)pyridin-4-yl)sulfanyl)propanoate | HCID 86731335 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-((2S)-1-((2-(4-hydroxyphenyl)[1,3]thiazolo[4,5-c]pyridin-6-yl)oxy)propan-2-yl)acetamide | HCID 136341406 | 89.5% |
Reaction Steps
A mixture of 2-ethylhexyl 3-((2-(((2S)-2-acetamidopropyl)oxy)-5-((4-(cyclopropylmethoxy)benzoyl)amino)pyridin-4-yl)sulfanyl)propanoate (740 mg), sodium ethoxide (20% ethanol solution, 840 mg) and THF (10 mL) was stirred at room temperature for 30 min. The reaction mixture was cooled to 0° C., trifluoroacetic acid (0.475 mL) was added thereto, the obtained mixture was stirred at 70° C. for 1 hr. The reaction mixture was cooled to 0° C., and the precipitate was collected by filtration, and washed with diisopropyl ether. The obtained residue was dissolved in trifluoroacetic acid (5 mL), and the obtained solution was stirred at 70° C. for 1 hr. The reaction mixture was added to saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. The combined organic layer were washed with saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure to give the title compound (379 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09133129B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-02ba7f13f7f9410786ca549879cf5fe7 |
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| Source note | uspto-grants-2015_09 |
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