HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1879713Generated: October 25, 2026
Water → 3-Chloro-5-[methyl(1-methylpropyl)amino]pyrazine-2-carbaldehyde
https://huagongshe.com/reaction/1879713
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 6-chloro-N-methyl-N-(1-methylpropyl)pyrazin-2-amine | HCID 61699767 | — |
| Product | 3-Chloro-5-[methyl(1-methylpropyl)amino]pyrazine-2-carbaldehyde | HCID 86648992 | 88% |
Reaction Steps
Phosphoryl chloride (1.33 mL) was added dropwise to DMF (5 mL) at 0° C. The mixture was stirred for 15 min, and a solution of 6-chloro-N-methyl-N-(1-methylpropyl)pyrazin-2-amine (1.43 g) in DMF (1 mL) was added dropwise thereto. The mixture was stirred at 80° C. for 18 hr, water (5 mL) was added at 0° C., and the mixture was stirred at room temperature for 1.5 hr. The mixture was extracted with ethyl acetate. The aqueous layer was extracted again with ethyl acetate. The combined organic layer was washed with water and saturated brine, dried over magnesium sulfate, and concentrated. The residue was purified by silica gel column chromatography (solvent gradient: 10→50% ethyl acetate/hexane) to give the title compound (1.43 g, 88%) as a pale-yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08318722B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-340d4e6ef23d478fa9aa649a1a970ad9 |
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| Source note | uspto-grants-2012_11 |
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