HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 418642Generated: October 30, 2026
Hydrochloric Acid → 3-Oxo-3-[(1,3-thiazol-2-yl)amino]propanoic acid
https://huagongshe.com/reaction/418642
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 2-Aminothiazole | HCID 2155 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | Methyl malonyl chloride | HCID 123460 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Oxolane--water (1/1) | HCID 21881883 | — |
| Product | 3-Oxo-3-[(1,3-thiazol-2-yl)amino]propanoic acid | HCID 12655699 | 69% |
Reaction Steps
To a solution of 2-aminothiazole (2.0 g, 19.97 mmol) in dry DCM (30 ml) at 0° C. was added TEA (4.03 g, 2 eq, 39.94 mmol) and methyl 3-chloro-3-oxopropanoate (3.0 g, 1.1 eq, 21.97 mmol). The reaction mixture was stirred for 1 hr at room temperature. The reaction mixture was concentrated to dryness, dissolved in EtOAc and washed well with water. The organic phase was collected, dried over anhydrous sodium sulfate then filtered and concentrated. The resultant solid was triturated with Et2O and used directly in the next step with no additional purification (1.1 g, 30% yield). To a solution of the ester 128 (500 mg, 2.49 mmol) in THF/water (1:1, 20 ml) was added LiOH×H2O (209 mg, 2 eq, 4.98 mmol) and the mixture stirred for 2 hrs at room temperature. The mixture was neutralized with 1 M HCl solution and adsorbed onto silica gel. Purification by column chromatography (60% EtOAc in hexanes) afforded the acid 129 as a white solid (320 mg, 69% yield). MS (m/z): 187.2 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08093264B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-5d43b5c08b9643b9848ad9f616cb794a |
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| Source note | uspto-grants-2012_01 |
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