HuagongsheHuagongshe Chemistry Print Report · For research reference only
P-Anisidine → 5,6-Dichloro-3-[(4-methoxyphenyl)imino]methylpyrazinamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | P-Anisidine | HCID 7732 | — |
| Reactant | 3-Amino-5,6-dichloropyrazine-2-carbaldehyde | HCID 13367871 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5,6-Dichloro-3-[(4-methoxyphenyl)imino]methylpyrazinamine | HCID 13367876 | — |
Reaction Steps
In a manner similar to that described in Example 9, 1.92 grams (0.01 mole) of 3-amino-5,6-dichloropyrazinaldehyde, 1.23 g (0.01 mole) of p-anisidine and 15 milliliters of ethanol were mixed together and heated at reflux temperature to obtain a 5,6-dichloro-3-[(4-methoxyphenyl)imino]methylpyrazinamine product which precipitated in the reaction mixture. The product was recovered by filtration, recrystallized from ethanol to obtain 2.14 grams of a purified product, m.p. 167°-168° C. (dec). Elemental analyses were as follows:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04479953 |
| Source dataset | uspto-grants-1984_10 |
| ORD ID | ord-e180cb2eaed342a69208ad1b5b66f797 |
| Source note | uspto-grants-1984_10 |