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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 661026Generated: October 27, 2026

Sulfuryl chloride → Methyl 2-amino-4-(methoxymethyl)thiazole-5-carboxylate

https://huagongshe.com/reaction/661026

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuryl chlorideHCID 24648—
ReactantMethyl 4-methoxyacetoacetateHCID 123500—
ReactantThioureaHCID 2723790—
ReactantMethyl 2-chloro-4-methoxy-3-oxobutanoateHCID 59295416—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
ProductMethyl 2-amino-4-(methoxymethyl)thiazole-5-carboxylateHCID 25220423—

Reaction Conditions

Temperature20 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084479B2
Source datasetuspto-grants-2011_12
ORD IDord-1dfcf4a8e04c45629996ab44e05a3ddb
Source noteuspto-grants-2011_12