HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methyl-2-oxovaleric acid → HCID 19104945, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methyl-2-oxovaleric acid | HCID 70 | — |
| Reactant | β,β-Diethoxy-3-pyridineethanamine | HCID 10987537 | — |
| Product | HCID 19104945 | HCID 19104945 | — |
Reaction Steps
In a manner analogous to Example 1, by condensing 3-(2-amino-1,1-diethoxyethyl)pyridine with 4-methyl-2-oxo-pentanoic acid there is obtained N-(2,2-diethoxy-2-(3-pyridyl)ethyl]-4-methyl2-oxovaleramide as a colorless, amorphous solid. Acidic hydrolysis yields 4-methyl-N-(nicotinoylmethyl)-2-oxovaleramide and subsequent ring closure yields 3-isobutyl-5-(3-pyridyl)-2(1H)-pyrazinone as a crystalline solid, melting point 195°-196° (from ethyl acetate). The conversion into the corresponding chloride, 2-chloro-3-isobutyl-5-(3-pyridyl)pyrazine, is also effected analogously to Example 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05278161 |
| Source dataset | uspto-grants-1994_01 |
| ORD ID | ord-44c66bc4b5be4d1790e645ce19b3640a |
| Source note | uspto-grants-1994_01 |