HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 567807Generated: October 30, 2026
Oxalyl chloride → Benzyl 2-[3,5-dichloro-2-methyl-6-oxo-1(6H)-pyrazinyl]acetate
https://huagongshe.com/reaction/567807
Participants
| Role | Name | HCID | Charge |
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| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Benzyl-2-[(1-cyanoethyl)amino]acetate hydrochloride | HCID 18470875 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Benzyl 2-[3,5-dichloro-2-methyl-6-oxo-1(6H)-pyrazinyl]acetate | HCID 10663926 | 41% |
Reaction Steps
A suspension of benzyl-2-[(1-cyanoethyl)amino]acetate hydrochloride (preparation 16) (17.8 g, 69.88 mmol) in toluene (120 ml) was treated cautiously with oxalyl chloride (24.38 ml). Once effervescence had ceased the reaction was heated at 100° C. (24 hr). The reaction was cooled, solvent evaporated to dryness and the resultant crude product purified by chromatography (SiO2, gradient elution with 70:30 pentane:ethyl acetate; 50:50 pentane:ethyl acetate; 30:70 pentane:ethyl acetate; 100% ethyl acetate). Chromatography again, (SiO2, eluting with 100% CH2Cl2) gave the desired product as an off-white solid (9.40 g, 41%). 1H NMR (CD3OD) δ 2.35 (s, 3H), 4.90 (s, 2H), 5.25 (s, 2H), 7.40 (m, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06180627B2 |
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| Source dataset | uspto-grants-2001_01 |
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| ORD ID | ord-01c05ba3ba1a4abc937e4f65a22905d7 |
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| Source note | uspto-grants-2001_01 |
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