HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 2-chloroacetoacetate → 5-chloro-6-methyl-1H-pyrimidin-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 2-chloroacetoacetate | HCID 11858 | — |
| Reactant | 4-Methoxybenzenecarboximidamide | HCID 229074 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 5-chloro-6-methyl-1H-pyrimidin-4-one | HCID 178433212 | 37.2% |
Reaction Steps
Under N2, a solution of ethyl 2-chloroacetoacetate (1.8 ml, d=1.15, 0.013 mol) in CHCl3 (50 ml) was added dropwise to a solution 4-methoxybenzamidine (3.9 g, 0.026 mol) in CHCl3 (100 ml). After stirring overnight, the reaction mixture was filtered and the filtrate was washed with dilute NaOH solution. The aqueous layer was extracted with CH2Cl2 (3×) and the organic layer was dried, filtered and concentrated to dryness. The residue was chromatographed on silica gel and the product was eluted with 2% CH3OH-CHCl3 (v/v) to yield 0.7 g (22%) of product m.p. 250°-251° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04598149 |
| Source dataset | uspto-grants-1986_07 |
| ORD ID | ord-467a2c405e6b411cb6e2def6ef2ec4b7 |
| Source note | uspto-grants-1986_07 |