HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243055Generated: November 1, 2026
Dimethylamine → Ethyl 2-Chloro-4-dimethylcarbamoyl-thiazole-5-carboxylate
https://huagongshe.com/reaction/2243055
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | 2,6-Lutidine | HCID 7937 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 2-Chloro-5-(ethoxycarbonyl)-1,3-thiazole-4-carboxylic acid | HCID 59208347 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 2-Chloro-4-dimethylcarbamoyl-thiazole-5-carboxylate | HCID 59208397 | 76% |
Reaction Steps
To a stirred solution of 2-chloro-5 (ethoxy carbonyl)-1,3-thiazole-4-carboxylic acid (Intermediate 7, 2 g, 8.01 mmol) in dry dichloromethane (20 mL) was added oxalyl chloride (1.37 mL, 16.02 mmol) and 2 drops of dry dimethylformamide. The reaction mixture was heated to 45° C. for 90 minutes. After the completion of the reaction, the reaction mixture was evaporated to dryness under reduced pressure. The residue was dissolved in dry dichloromethane (20 mL) and was cooled to 0° C., then 2,6-lutidine (0.97 mL, 8.4 mmol) was added followed by addition of N,N-dimethylamine (2 M solution in tetra hydro furan, 4.19 mL, 8.4 mmol). After completion of the reaction, the reaction mixture was concentrated to dryness and the residue was extracted with ethyl acetate (2×50 mL). The organic layer was washed with 1 N hydrochloric acid, water and brine (1×50 mL), and concentrated after drying over anhydrous sodium sulfate to afford 1.6 g (72.7%) of the title compound as a thick syrup.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07674801B2 |
|---|
| Source dataset | uspto-grants-2010_03 |
|---|
| ORD ID | ord-a045682d867f43f092cd74971b0872bd |
|---|
| Source note | uspto-grants-2010_03 |
|---|