HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanoacetamide → 4-Cyano-2,3,5,6,7,8-hexahydro-7-methoxy-1-methyl-3-oxoisoquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanoacetamide | HCID 7898 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 2-Acetyl-4-methoxycyclohexanone | HCID 13632724 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Cyano-2,3,5,6,7,8-hexahydro-7-methoxy-1-methyl-3-oxoisoquinoline | HCID 13632726 | 35% |
Reaction Steps
1.02 g of 2-acetyl-4-methoxycyclohexanone and 0.462 g of cyanoacetamide were mixed with 5 ml of ethanol and a small amount of piperidine was added thereto. The obtained reaction mixture was heated under reflux for two hours. The crystals thus precipitated were filtered and recrystallized from methanol to give 0.42 g of 4-cyano-2,3,5,6,7,8-hexahydro-7-methoxy-1-methyl-3-oxoisoquinoline. m.p. 257°-259° C. NMRTMSCF3COOH : 2.25 (2H, m), 2.57 (3H, s), 2.97 (2H, m), 3.20 (2H, m), 3.66 (3H, s) and 4.16 (1H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04824952 |
| Source dataset | uspto-grants-1989_04 |
| ORD ID | ord-d2208649ebda4198a0a180cb62ab453e |
| Source note | uspto-grants-1989_04 |