HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2109699Generated: October 27, 2026
Sulfuryl chloride → Methyl 2-amino-4-(methoxymethyl)thiazole-5-carboxylate
https://huagongshe.com/reaction/2109699
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | Methyl 4-methoxyacetoacetate | HCID 123500 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | Methyl 2-chloro-4-methoxy-3-oxobutanoate | HCID 59295416 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 2-amino-4-(methoxymethyl)thiazole-5-carboxylate | HCID 25220423 | — |
Reaction Steps
To a 100 mL round-bottomed flask was added methyl 4-methoxy-3-oxobutanoate (4.43 mL, 34.2 mmol) and DCM (30.00 mL). Sulfuryl chloride (2.91 mL, 35.9 mmol) was added dropwise with a syringe to the reaction mixture. The mixture was then stirred for 1 hour at 20° C. The solution was reduced to an oil under reduced pressure and dissolved in EtOH (50 mL). To this solution was added methyl 2-chloro-4-methoxy-3-oxobutanoate (6.18 g, 34 mmol) and thiourea (1.9 mL, 34 mmol). The reaction was then stirred at reflux for approximately 12 hours. LCMS indicated that the reaction was complete, and the solvent was removed under reduced pressure. Saturated aqueous sodium bicarbonate was added, and the resulting solid was filtered and recrystallized from water and <5 mL EtOH to give methyl 2-amino-4-(methoxymethyl)thiazole-5-carboxylate as rust colored crystals (4.85 g, 68%). LCMS (M+H) 203 calc. for C7H11N2O3S 203.2. 1H NMR (400 MHz, CD3OD): δ ppm 4.64 (s, 2H), 3.77 (s, 3H), 3.37 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07514566B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-ac5bcc70626545ad90ff23822bda1949 |
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| Source note | uspto-grants-2009_04 |
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