HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 127683Generated: October 25, 2026
Dimethylformamide → HCID 178496340, compound
https://huagongshe.com/reaction/127683
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 2-Methoxyethyl chloroformate | HCID 69400 | — |
| Reactant | HCID 178507684 | HCID 178507684 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 178496340 | HCID 178496340 | — |
Reaction Steps
5 G. of 2,4-diamino-6-chloropyrimidine-3-oxide are suspended in 50 ml. of dimethylformamide and 5 ml. of triethylamine and cooled to 0° C. while stirring. 4.3 G. of chloroformic acid 2-methoxyethyl ester are added dropwise to the cold suspension in the course of 15 minutes. The mixture is cooled for 2 hours and then stirred at room temperature for 16 hours. The solvent is distilled off at 25° C. in a high vacuum and the residue is digested with methylene chloride. The precipitate obtained is filtered off and washed with methylene chloride, methanol and water. The filtrate is washed with water and dried over sodium sulfate. By concentrating the solvent, there is obtained pure 2-methoxyethyl 2-amino-6-chloro-4-pyrimidinecarbamate-3-oxide having a melting point of 176°-178° C. Additional material is obtained by subjecting the mother liquor to chromatographical separation on silica gel.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04256886 |
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| Source dataset | uspto-grants-1981_03 |
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| ORD ID | ord-1a321ca1ba284e5c9a05ac59db3a1ea5 |
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| Source note | uspto-grants-1981_03 |
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