HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1971690Generated: October 25, 2026
Hydrochloric Acid → 2-(Tert-butyl-(2-(3-(thiazol-5-yl)prop-2-ynyloxy)ethyl)amino)-2-oxoacetic acid
https://huagongshe.com/reaction/1971690
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Ethyl 2-(tert-butyl(2-(3-(thiazol-5-yl)prop-2-ynyloxy)ethyl)amino)-2-oxoacetate | HCID 58124907 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-(Tert-butyl-(2-(3-(thiazol-5-yl)prop-2-ynyloxy)ethyl)amino)-2-oxoacetic acid | HCID 58124930 | 104.2% |
Reaction Steps
A solution of 450 mg of 11e in 4 ml of dioxane was mixed with a solution of 250 mg of KOH in 2 ml of water and stirred at 55° C. for 1 h. The reaction mixture was then cooled and diluted with 20 ml of water and made acidic to pH3 by addition of 0.5N HCl. The product was extracted with ethyl acetate. The organic extract was washed once with water, dried and concentrated, to give 430 mg of 11f as a colorless oil, which solidified on standing; Mp: 104-105° C.; Rf 0.20 (CH2Cl2/methanol 8/2). MS-ESI:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08431564B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-621bc18995544258bd6561c06d149bd1 |
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| Source note | uspto-grants-2013_04 |
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