HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2188673Generated: October 29, 2026
Water → 5-[Benzyl(1-methylethyl)amino]-3-chloropyrazine-2-carbaldehyde
https://huagongshe.com/reaction/2188673
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | N-benzyl-6-chloro-N-(1-methylethyl)pyrazin-2-amine | HCID 61699183 | — |
| Product | 5-[Benzyl(1-methylethyl)amino]-3-chloropyrazine-2-carbaldehyde | HCID 86648999 | 70% |
Reaction Steps
Phosphoryl chloride (5.6 mL) was added dropwise to DMF (12 mL) at 0° C. The mixture was stirred for 15 min, and a solution of N-benzyl-6-chloro-N-(1-methylethyl)pyrazin-2-amine (3.40 g) in DMF (3 mL) was added dropwise thereto. The mixture was stirred at 100° C. for 13 hr, water (50 mL) was added at 0° C., and the mixture was stirred at room temperature for 1 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: 5→20% ethyl acetate/hexane) to give the title compound (2.42 g, 70%) as a pale-yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08324201B2 |
|---|
| Source dataset | uspto-grants-2012_12 |
|---|
| ORD ID | ord-7ee05bc0c1cf4af298525e3ed6272370 |
|---|
| Source note | uspto-grants-2012_12 |
|---|